https://recall-ledger-cue.pages.dev/ Recall Ledger tracks every product recall published by the FDA, USDA FSIS, CPSC and NHTSA, and rewrites each one into a page that tells you what was pulled, which lot codes and UPCs are affected, where it sold, and how to get your money back. en-us Sat, 24 Oct 2026 12:00:00 GMT https://recall-ledger-cue.pages.dev/recall/imperio-distribution-llc-beef-jerky-products-produced-with-u027-2026 https://recall-ledger-cue.pages.dev/recall/imperio-distribution-llc-beef-jerky-products-produced-with-u027-2026 Sat, 24 Oct 2026 12:00:00 GMT Food & beverages Produced Without Benefit of Inspection Produced Without Benefit of Inspection https://recall-ledger-cue.pages.dev/recall/vqqq-natural-gas-patio-heaters-recall-components-on-the-re-c11028 https://recall-ledger-cue.pages.dev/recall/vqqq-natural-gas-patio-heaters-recall-components-on-the-re-c11028 Thu, 22 Oct 2026 12:00:00 GMT Consumer products Components on the recalled patio heaters can malfunction, causing gas to be released, posing a risk of serious injury or death from fire and burn hazards. Components on the recalled patio heaters can malfunction, causing gas to be released, posing a risk of serious injury or death from fire and burn hazards. https://recall-ledger-cue.pages.dev/recall/lithonia-lighting-rsx-luminaires-with-adjustable-tilt-arm-c11029 https://recall-ledger-cue.pages.dev/recall/lithonia-lighting-rsx-luminaires-with-adjustable-tilt-arm-c11029 Thu, 22 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury from Impact Hazard The knuckle of the recalled adjustable tilt arm mountings can fail, allowing the luminaire to fall from the mounting arm, posing a risk of serious injury due to impact hazard. https://recall-ledger-cue.pages.dev/recall/foshanshinanhaiqunuoaitongzhuangshanghang-ciyti-light-up-p-c11032 https://recall-ledger-cue.pages.dev/recall/foshanshinanhaiqunuoaitongzhuangshanghang-ciyti-light-up-p-c11032 Thu, 22 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys The costumes violate the mandatory safety standard for toys because the button cell batteries can be accessed easily by children, posing a deadly ingestion hazard. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death. https://recall-ledger-cue.pages.dev/recall/costway-convertible-high-chairs-recall-risk-of-serious-inj-c11030 https://recall-ledger-cue.pages.dev/recall/costway-convertible-high-chairs-recall-risk-of-serious-inj-c11030 Thu, 22 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for High Chairs The convertible high chairs violate the mandatory safety standard for high chairs because they do not contain a passive restraint system and a child can slip through the opening between the feeding tray and seat and become entrapped or fall, posing a risk of serious injury or death. https://recall-ledger-cue.pages.dev/recall/bamamon-led-projecting-finger-light-toys-recall-risk-of-se-c11031 https://recall-ledger-cue.pages.dev/recall/bamamon-led-projecting-finger-light-toys-recall-risk-of-se-c11031 Thu, 22 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys None reported. https://recall-ledger-cue.pages.dev/recall/audi-q4-e-tron-recall-the-high-voltage-battery-may-fail-an-v26v698000 https://recall-ledger-cue.pages.dev/recall/audi-q4-e-tron-recall-the-high-voltage-battery-may-fail-an-v26v698000 Wed, 21 Oct 2026 12:00:00 GMT Vehicles & equipment The high voltage battery may fail and cause a fire. A vehicle fire increases the risk of injury. https://recall-ledger-cue.pages.dev/recall/kayem-foods-inc-meat-and-poultry-products-due-to-possible-u026-2026 https://recall-ledger-cue.pages.dev/recall/kayem-foods-inc-meat-and-poultry-products-due-to-possible-u026-2026 Sat, 17 Oct 2026 12:00:00 GMT Food & beverages Processing Defect Processing Defect https://recall-ledger-cue.pages.dev/recall/volvo-vnl-recall-the-truck-cabs-may-have-loose-or-missing-v26v677000 https://recall-ledger-cue.pages.dev/recall/volvo-vnl-recall-the-truck-cabs-may-have-loose-or-missing-v26v677000 Thu, 15 Oct 2026 12:00:00 GMT Vehicles & equipment The truck cabs may have loose or missing structural bolts. A cab with loose or missing structural bolts may not properly protect an occupant during a crash, increasing the risk of injury. https://recall-ledger-cue.pages.dev/recall/usopal-xalirium-portable-bed-rails-recall-risk-of-serious-c11025 https://recall-ledger-cue.pages.dev/recall/usopal-xalirium-portable-bed-rails-recall-risk-of-serious-c11025 Thu, 15 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap… https://recall-ledger-cue.pages.dev/recall/primark-101-dalmatians-faux-leather-childrens-coin-purses-c11027 https://recall-ledger-cue.pages.dev/recall/primark-101-dalmatians-faux-leather-childrens-coin-purses-c11027 Thu, 15 Oct 2026 12:00:00 GMT Consumer products Phthalate Levels and Risk of Ingestion The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through ingestion, and certain phthalates have been associated with adverse health effects, particularly effects on development and the hormone system. https://recall-ledger-cue.pages.dev/recall/papablic-of-usa-convertible-bedside-sleepers-recall-risk-o-c11024 https://recall-ledger-cue.pages.dev/recall/papablic-of-usa-convertible-bedside-sleepers-recall-risk-o-c11024 Thu, 15 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby to become entrapped between the sleeping pad and bottom posing a deadly suffocation hazard. In addition, the latching and locking mechanism can fail, causing the product to collapse, posing a risk of serious injury or… https://recall-ledger-cue.pages.dev/recall/loving-thyself-rocks-crystal-glass-cups-recall-risk-of-ser-c11023 https://recall-ledger-cue.pages.dev/recall/loving-thyself-rocks-crystal-glass-cups-recall-risk-of-ser-c11023 Thu, 15 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury from Ingestion and Laceration Hazards Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards. https://recall-ledger-cue.pages.dev/recall/hatsanusa-blitz-air-rifles-recall-risk-of-serious-injury-o-c11026 https://recall-ledger-cue.pages.dev/recall/hatsanusa-blitz-air-rifles-recall-risk-of-serious-injury-o-c11026 Thu, 15 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury or Death from Projectile Hazard The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from projectile hazard. https://recall-ledger-cue.pages.dev/recall/3m-company-scotchtm-thermal-laminators-recall-risk-of-seri-c11022 https://recall-ledger-cue.pages.dev/recall/3m-company-scotchtm-thermal-laminators-recall-risk-of-seri-c11022 Thu, 15 Oct 2026 12:00:00 GMT Consumer products Risk of Serious Injury or Death from Fire Hazard The recalled thermal laminators can overheat, posing a fire hazard. https://recall-ledger-cue.pages.dev/recall/toyota-land-cruiser-hybrid-recall-the-fuel-tube-connection-v26v673000 https://recall-ledger-cue.pages.dev/recall/toyota-land-cruiser-hybrid-recall-the-fuel-tube-connection-v26v673000 Wed, 14 Oct 2026 12:00:00 GMT Vehicles & equipment The fuel tube connection near the fuel tank may disconnect and leak fuel. A fuel leak in the presence of an ignition source can increase the risk of a fire. https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-plastics-tray-recall-product-may-be-poten-mz-0100-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-plastics-tray-recall-product-may-be-poten-mz-0100-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-passport-series-patient-monitor-operato-mz-0114-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-passport-series-patient-monitor-operato-mz-0114-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-heart-prep-tray-recall-product-may-be-pot-mz-0102-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-heart-prep-tray-recall-product-may-be-pot-mz-0102-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-pack-open-heart-cfh-recall-product-may-be-mz-0097-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-pack-open-heart-cfh-recall-product-may-be-mz-0097-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/lemaitre-vascular-inc-tuftex-over-the-wire-embolectomy-cat-mz-0117-2027-99836 https://recall-ledger-cue.pages.dev/recall/lemaitre-vascular-inc-tuftex-over-the-wire-embolectomy-cat-mz-0117-2027-99836 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing. Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing. https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-t1-patient-monitor-operators-manual-t1-mz-0116-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-t1-patient-monitor-operators-manual-t1-mz-0116-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/drg-international-inc-sperm-ab-elisa-recall-potential-for-mz-0082-2027-99799 https://recall-ledger-cue.pages.dev/recall/drg-international-inc-sperm-ab-elisa-recall-potential-for-mz-0082-2027-99799 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Potential for false negative patient results. Potential for false negative patient results. https://recall-ledger-cue.pages.dev/recall/intellijoint-navigation-system-workstation-g2-configured-r-mz-0119-2027-99821 https://recall-ledger-cue.pages.dev/recall/intellijoint-navigation-system-workstation-g2-configured-r-mz-0119-2027-99821 Wed, 14 Oct 2026 12:00:00 GMT Medical devices A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an Apple battery recall, that may overheat and pose a fire safety risk. A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an Apple battery recall, that may overheat and pose a fire safety risk. https://recall-ledger-cue.pages.dev/recall/quantum-ops-inc-brand-name-adaptable-beach-chair-product-n-mz-0076-2027-99384 https://recall-ledger-cue.pages.dev/recall/quantum-ops-inc-brand-name-adaptable-beach-chair-product-n-mz-0076-2027-99384 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Due to a manufacturing issue (inadequate weld) for patient head positioning system. Due to a manufacturing issue (inadequate weld) for patient head positioning system. https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-laparoscopic-prostatectomy-recall-product-mz-0099-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-laparoscopic-prostatectomy-recall-product-mz-0099-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-beneview-series-operators-manuals-t5-t8-mz-0113-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-beneview-series-operators-manuals-t5-t8-mz-0113-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-cpm-series-patient-monitor-operators-ma-mz-0115-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-cpm-series-patient-monitor-operators-ma-mz-0115-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/beckman-coulter-inc-dxc-500-au-clinical-chemistry-analyzer-mz-0084-2027-99800 https://recall-ledger-cue.pages.dev/recall/beckman-coulter-inc-dxc-500-au-clinical-chemistry-analyzer-mz-0084-2027-99800 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to use units different from the system default, a subsequent configuration change and activation of the draft configuration in the System Configuration page may cause the analyzer to revert the test units to the system default setting without notifying the user. The system does Pre-Review Reminders Include OII and… https://recall-ledger-cue.pages.dev/recall/canon-medical-system-usa-inc-alphenix-infx-8000c-b5-recall-mz-0108-2027-99817 https://recall-ledger-cue.pages.dev/recall/canon-medical-system-usa-inc-alphenix-infx-8000c-b5-recall-mz-0108-2027-99817 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and a longitudinal motion error Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and a longitudinal motion error https://recall-ledger-cue.pages.dev/recall/gri-medical-and-electronic-technology-co-ltd-halyard-lapar-mz-0077-2027-99813 https://recall-ledger-cue.pages.dev/recall/gri-medical-and-electronic-technology-co-ltd-halyard-lapar-mz-0077-2027-99813 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-endovascular-pack-recall-product-may-be-p-mz-0095-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-endovascular-pack-recall-product-may-be-p-mz-0095-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-benevision-series-telemetry-monitor-ope-mz-0111-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-benevision-series-telemetry-monitor-ope-mz-0111-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-davinci-lap-gyn-recall-product-may-be-pot-mz-0101-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-davinci-lap-gyn-recall-product-may-be-pot-mz-0101-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/polymedco-inc-polymedco-cancer-diagnostic-products-llc-sed-mz-0107-2027-99810 https://recall-ledger-cue.pages.dev/recall/polymedco-inc-polymedco-cancer-diagnostic-products-llc-sed-mz-0107-2027-99810 Wed, 14 Oct 2026 12:00:00 GMT Medical devices During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach or be forcibly ejected, potentially resulting in the release of blood and exposure of the operator or surrounding work area to a biological hazard (blood). During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach… https://recall-ledger-cue.pages.dev/recall/beckman-coulter-inc-dxc-500i-clinical-analyzer-modules-1-d-mz-0083-2027-99800 https://recall-ledger-cue.pages.dev/recall/beckman-coulter-inc-dxc-500i-clinical-analyzer-modules-1-d-mz-0083-2027-99800 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to use units different from the system default, a subsequent configuration change and activation of the draft configuration in the System Configuration page may cause the analyzer to revert the test units to the system default setting without notifying the user. The system does Pre-Review Reminders Include OII and… https://recall-ledger-cue.pages.dev/recall/cardinal-health-200-llc-presource-packs-containing-medtron-mz-0079-2027-99801 https://recall-ledger-cue.pages.dev/recall/cardinal-health-200-llc-presource-packs-containing-medtron-mz-0079-2027-99801 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the patient's endotracheal tube to perform a procedure. The issue can result in a delay to treatment and unintended extubation. The potential exists for respiratory failure, hypoxia, aspiration, or low oxygen saturation. Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these… https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-panorama-and-telemetry-monitoring-syste-mz-0112-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-panorama-and-telemetry-monitoring-syste-mz-0112-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-major-pack-recall-product-may-be-potentia-mz-0104-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-major-pack-recall-product-may-be-potentia-mz-0104-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/medical-action-industries-inc-306-generic-name-kit-urine-c-mz-0069-2027-99491 https://recall-ledger-cue.pages.dev/recall/medical-action-industries-inc-306-generic-name-kit-urine-c-mz-0069-2027-99491 Wed, 14 Oct 2026 12:00:00 GMT Medical devices An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027. An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027. https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-gyn-laparoscopy-laparotomy-recall-product-mz-0093-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-gyn-laparoscopy-laparotomy-recall-product-mz-0093-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-benevision-n1-and-n-series-patient-moni-mz-0110-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-benevision-n1-and-n-series-patient-moni-mz-0110-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-abd-hysterectomy-recall-product-may-be-po-mz-0106-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-abd-hysterectomy-recall-product-may-be-po-mz-0106-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-gyn-laparoscopy-pack-recall-product-may-b-mz-0105-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-gyn-laparoscopy-pack-recall-product-may-b-mz-0105-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/medline-industries-lp-rollator-bariatric-basic-steel-burgu-mz-0086-2027-99807 https://recall-ledger-cue.pages.dev/recall/medline-industries-lp-rollator-bariatric-basic-steel-burgu-mz-0086-2027-99807 Wed, 14 Oct 2026 12:00:00 GMT Medical devices The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the front wheels may become loose or detach from the rollator. If the front wheels become loose or detach during use, there is risk of severe adverse events. The immediate consequences could include falls resulting in head trauma, bone fractures, or other critical injuries. The front fork stem bolt/wheel assembly may… https://recall-ledger-cue.pages.dev/recall/steris-corporation-verify-biological-steam-test-pack-model-mz-0075-2027-99704 https://recall-ledger-cue.pages.dev/recall/steris-corporation-verify-biological-steam-test-pack-model-mz-0075-2027-99704 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor… https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-davinci-trucustom-bundle-recall-product-m-mz-0092-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-davinci-trucustom-bundle-recall-product-m-mz-0092-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-epm-series-patient-monitor-patient-moni-mz-0109-2027-99828 https://recall-ledger-cue.pages.dev/recall/mindray-ds-usa-inc-epm-series-patient-monitor-patient-moni-mz-0109-2027-99828 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-urology-major-recall-product-may-be-poten-mz-0103-2027-99808 https://recall-ledger-cue.pages.dev/recall/avid-medical-inc-urology-major-recall-product-may-be-poten-mz-0103-2027-99808 Wed, 14 Oct 2026 12:00:00 GMT Medical devices Product may be potentially contaminated with a lubricant used during the manufacturing process. Product may be potentially contaminated with a lubricant used during the manufacturing process. https://recall-ledger-cue.pages.dev/recall/steris-corporation-hexavue-focus-integration-system-a-sing-mz-0118-2027-99856 https://recall-ledger-cue.pages.dev/recall/steris-corporation-hexavue-focus-integration-system-a-sing-mz-0118-2027-99856 Wed, 14 Oct 2026 12:00:00 GMT Medical devices A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a documentation discrepancy or incorrect association of clinical images with a patient record. A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a documentation discrepancy or incorrect association of…