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. 1,098 recalls have been distributed to New York in the last 12 months.
Showing 18021–18040 of 55,896 recalls
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dental pins - TMS LINK PLUS Self-Threading Pins - Product Recalled by...
The Issue: The incorrect dental pins were packaged and subsequently distributed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Processor SP - Product Usage: intended for processing and Recalled...
The Issue: Potential for a false-negative result for Vibrio parahaemolyticus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentueri Viral Transport Medium (VTM) Recalled by Gentueri Inc Due to Medium...
The Issue: Medium showed visual turbidity and discoloration, potentially contaminating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBplus and AquaBplus B2 Water Purification System - Product Usage:...
The Issue: AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #:...
The Issue: Discrepancy in labeling between the adult CBC ranges presented in the OLO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...
The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Martin-Lewis Agar Recalled by Becton Dickinson & Co. Due to Products...
The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Captia Measles IgM Kit Recalled by Clark Laboratories, Inc....
The Issue: Positive Control may run high out of its assigned ISR range and result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Enterprise Viewer Recalled by CHANGE HEALTHCARE CANADA...
The Issue: Change Healthcare has identified an intermittent software defect which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal...
The Issue: Incorrect labeling, Catheter did not have the required holes and markings
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telmisartan Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label-mixup
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.