Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,820 recalls have been distributed to New York in the last 12 months.
Showing 11721–11740 of 30,153 recalls
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare Recalled by RAYSEARCH LABORATORIES AB Due to When performing offline...
The Issue: When performing offline image review in RayCare 2C, RayCare 3A and RayCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Control Recalled by Medline Industries Inc Due to Product was shipped with...
The Issue: Product was shipped with (ice) instead of frozen (dry ice).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Removal Case Assembly Recalled by Wright Medical Technology, Inc. Due...
The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardware removal kit Recalled by Wright Medical Technology, Inc. Due to...
The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JINYINSHAN Recalled by Office Depot Inc Due to Test results revealed that...
The Issue: Test results revealed that the KN95 masks failed to filter greater than 95%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Recalled by...
The Issue: Kits were packaged with the incorrect size valve peelable introducer. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Recalled by C.A....
The Issue: Sample leaking from the sleeve covering the needle inside the cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 34cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.