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. 2,889 recalls have been distributed to New York in the last 12 months.
Showing 3181–3200 of 55,896 recalls
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Walgreens Recalled by Sigan Industries Group Inc. Due to Chemical...
The Issue: Chemical Contamination: Presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...
The Issue: Potential for the gold unlock button to separate from the inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoroptor VRx Digital System Model Numbers: 16241 Recalled by Reichert, Inc....
The Issue: The head of the phoropter head could come loose and potentially detach due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoroptor VRx Digital System Model Numbers: 16242 Recalled by Reichert, Inc....
The Issue: The head of the phoropter head could come loose and potentially detach due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...
The Issue: Potential for the gold unlock button to separate from the inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...
The Issue: Potential for the gold unlock button to separate from the inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monterey AL Implant Inserter Recalled by Stryker Spine Due to Potential for...
The Issue: Potential for the gold unlock button to separate from the inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...
The Issue: Stability data does not support expiry: the products have the potential to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neupogen (filgrastim) For Injection Recalled by Amgen, Inc. Due to Stability...
The Issue: Stability data does not support expiry: the products have the potential to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: t:slim X2 Insulin Pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tandem Mobi Insulin Pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in Version 7.9 of the pump software for Tandem t:slim X2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Solo Diamond - Large Invented Cone Recalled by Premier Dental...
The Issue: The hardness not meeting the material specification and may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: MyDay Toric Recalled by CooperVision, Inc. Due to a limited...
The Issue: a limited number of lots were manufactured with an incorrect cylinder power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LPS Flex Recalled by Zimmer, Inc. Due to The "Use with plate 7, 8, 9,...
The Issue: The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration...
The Issue: Aspiration catheter distal tip features and characteristics may not be in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...
The Issue: Beckman Coulter has determined that device software versions V1.3, V1.4,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Da Vinci 5 Product Name: ASSY Recalled by Intuitive Surgical,...
The Issue: Due to an increase in complaints concerning foot tray pedal spring failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.