Recalls affecting Indiana
Notices that name Indiana in their distribution area, plus every nationwide recall — nationwide recalls reach Indiana too.
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High - Class I · yesterday
Imperio Distribution LLC Beef Jerky products recall: Produced Without Benefit of Inspection
Produced Without Benefit of Inspection
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Highest risk · 3 days ago
Lithonia Lighting RSX Luminaires with Adjustable Tilt Arm Mountings recall: Risk of Serious Injury from Impact Hazard
Risk of Serious Injury from Impact Hazard
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Highest risk · 3 days ago
Costway Convertible High Chairs recall: Risk of Serious Injury or Death from Entrapment and Fall Hazards
Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for High Chairs
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NHTSA safety recall · 4 days ago
Audi Q4 E-TRON recall: The high voltage battery may fail and cause a fire
The high voltage battery may fail and cause a fire.
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High - Class I · 8 days ago
Kayem Foods Inc. Meat and Poultry products recall: Processing Defect
Processing Defect
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NHTSA safety recall · 10 days ago
Volvo VNL recall: The truck cabs may have loose or missing structural bolts
The truck cabs may have loose or missing structural bolts.
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Highest risk · 10 days ago
HatsanUSA Blitz Air Rifles recall: Risk of Serious Injury or Death from Projectile Hazard
Risk of Serious Injury or Death from Projectile Hazard
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NHTSA safety recall · 11 days ago
Toyota Land Cruiser Hybrid recall: The fuel tube connection near the fuel tank may disconnect and leak fuel
The fuel tube connection near the fuel tank may disconnect and leak fuel.
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Class II · 11 days ago
AVID Medical, Inc. Plastics Tray 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. Passport Series Patient Monitor. Operator's Manuals: 8 / 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
AVID Medical, Inc. Heart Prep Tray 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. Pack Open Heart CFH 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
LeMaitre Vascular, Inc. TufTex¿ Over-the-Wire Embolectomy Catheter recall: Devices failed in process testing related to the amount of pull force it
Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.
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Class III · 11 days ago
Mindray DS USA, Inc. T1 Patient Monitor. Operator's Manual: T1 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
DRG International, Inc. Sperm Ab ELISA recall: Potential for false negative patient results
Potential for false negative patient results.
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Class II · 11 days ago
Intellijoint recall: A navigation system used to aid in selection and positioning of orthopedic
A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch…
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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.