Latest recalls — page 2
Older notices, newest first.
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Class II · 11 days ago
QUANTUM OPS Inc Brand Name: Adaptable Beach Chair Product Name: Beach Chair surgical recall: Due to a manufacturing issue (inadequate weld) for patient head positioning
Due to a manufacturing issue (inadequate weld) for patient head positioning system.
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Class II · 11 days ago
AVID Medical, Inc. Laparoscopic Prostatectomy recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class III · 11 days ago
Mindray DS USA, Inc. BeneView Series. Operator's Manuals: T5 / T8 recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
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Class III · 11 days ago
Mindray DS USA, Inc. cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12 recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
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Class II · 11 days ago
Beckman Coulter Inc. DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE recall: Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical
Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical Analyzers when testing plasma samples. Following user configuration of…
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Class II · 11 days ago
Canon Medical System, USA, INC. Alphenix INFX-8000C/B5 recall: Loosening of the bolts securing the longitudinal movement mechanism may cause
Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient]…
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Class II · 11 days ago
GRI Medical & Electronic Technology Co., Ltd. Halyard Laparoscopy Comprehensive Pack recall: Laparoscopy packs labeled as "latex free" were found to contain a latex
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
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Class II · 11 days ago
AVID Medical, Inc. Endovascular Pack recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class III · 11 days ago
Mindray DS USA, Inc. BeneVision Series Telemetry Monitor. Operator's Manuals recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
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Class II · 11 days ago
AVID Medical, Inc. Davinci LAP/GYN recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class II · 11 days ago
Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC Sediplast recall: During use of an affected tube, the operator may encounter increased
During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause…
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Class II · 11 days ago
Beckman Coulter Inc. DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE recall: Beckman Coulter has identified a software issue affecting DxC 500i Clinical
Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a…
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Class II · 11 days ago
Cardinal Health 200, LLC Presource Packs containing Medtronic Microstream Components recall: Kits contain Microstream components. Medtronic issued an update
Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in…
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Class III · 11 days ago
Mindray DS USA, Inc. Panorama and Telemetry Monitoring System. Operator's Manuals recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
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Class II · 11 days ago
AVID Medical, Inc. Major Pack recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class III · 11 days ago
Medical Action Industries, Inc. 306 recall: An internal data-entry error caused kit lot 333606 to be labeled
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.
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Class II · 11 days ago
AVID Medical, Inc. GYN Laparoscopy/Laparotomy recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class III · 11 days ago
Mindray DS USA, Inc. BeneVision N1 and N-Series Patient Monitor. Patient Monitor recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
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Class II · 11 days ago
AVID Medical, Inc. ABD Hysterectomy recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class II · 11 days ago
AVID Medical, Inc. GYN Laparoscopy Pack recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class II · 11 days ago
Medline Industries, LP Rollator, Bariatric, Basic Steel, Burgundy recall: The front fork stem bolt/wheel assembly may disconnect from the rollator
The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from…
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Class II · 11 days ago
Steris Corporation Verify Biological Steam Test Pack Model/ recall: Geobacillus stearothermophilus spore population in affected products may fall
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam…
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Class II · 11 days ago
AVID Medical, Inc. Davinci Trucustom Bundle recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
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Class III · 11 days ago
Mindray DS USA, Inc. ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…