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. 2,689 recalls have been distributed to New York in the last 12 months.
Showing 21301–21320 of 30,153 recalls
Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...
The Issue: Potential for polystyrene particulate presence.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT Flow 20-3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH 64-4R TruePoint w/TrueV Recalled by Siemens Medical Solutions USA...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT Flow Edge-3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint TV Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...
The Issue: Potential for polystyrene particulate presence.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH 40 - 3 Ring Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH 40 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...
The Issue: Potential for polystyrene particulate presence.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...
The Issue: Potential for polystyrene particulate presence.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Sys 16-3R to 16-4R upgrade Recalled by Siemens Medical Solutions...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT S(20)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...
The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...
The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.