Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

20151–20175 of 27647

HighFDA (Devices)·Z-1235-2017·2017-03-01
Terumo Sarns Centrifugal Pump Recalled for Housing Cracks and Leaks
Terumo is recalling Sarns Centrifugal Pumps because cracks in the housing can cause fluid leaks during cardiac procedures. No patient injuries have been reported.
Product
The Sarns Centrifugal Pump is a single use device sterilized by ethylene oxide gas. The device is sold single sterile in cartons of 8 units, or may be provided in bulk, non-sterile to another Terumo location for inclusion in Cardiovascular Procedure Kits. Cardiovascular…
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1161-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1172-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1225-2017·2017-03-01
Tosoh HLC-723G8 Analyzer Recalled for HbA1c Test Inaccuracy
Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.
Product
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1174-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1157-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1228-2017·2017-03-01
Arrow International Recalls Vascular Catheter Introduction Kits Due to Flaring Sheaths
Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.
Product
Vascular catheter introduction kit The PICC is indicated for short or long term peripheral access to the central Venous system for intravenous therapy, blood sampling, infusion and power injection of contrast media.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1152-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee System Tibial Resector Body Tubes and Guides due to potential alumina inclusions that could cause the instruments to crack or separate.
Product
Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1173-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1159-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1170-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 1 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1158-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1169-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1154-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1229-2017·2017-03-01
Philips Efficia CMS200 Central Monitoring System Recalled for Pediatric Alarm Defect
Philips is recalling 156 Efficia CMS200 central monitoring systems because they may not alarm appropriately for pediatric or neonatal patients.
Product
Philips Efficia CMS200 Central Monitoring System; 863352 The Efficia CMS200 central monitoring system is intended for use by healthcare professionals for central viewing of physiologic waves, parameters, and trends from other networked medical devices (patient monitors and…
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1233-2017·2017-03-01
Degania Silicone Jackson-Pratt Drain Recalled for Sterility Compromise
Degania Silicone is recalling 3,040 units of Jackson-Pratt Channel Drain Silicone Round because the sterile barrier was breached, compromising sterility.
Product
Jackson-Pratt Channel Drain Silicone Round, Fully Fluted w/10FR Trocar. Sterile. Rx Distributed by Cardinal Health, USA Catalog Number: JP-2187 For wound drainage.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1162-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1160-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1166-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1168-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 3 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1155-2017·2017-03-01
Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1153-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System Femoral Slap Hammers due to potential alumina inclusions that could cause the instruments to crack or separate.
Product
Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1171-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1156-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1175-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states

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20151–20175 of 27647