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. 2,619 recalls have been distributed to New York in the last 12 months.
Showing 35461–35480 of 55,896 recalls
Recalled Item: 4C All Natural Parmesan/Romano Grated Cheese Recalled by 4 C Foods, Corp....
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C All Natural 100% Imported Italian Pecorino Romano Cheese Recalled by 4 C...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C Homestyle All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp....
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cento Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cento Romano Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...
The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy 4 Implant Recalled by Implant Direct Sybron...
The Issue: The vial cap was mislabeled with the incorrect part number of 855708 but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...
The Issue: Failed Stability Specifications; out-of specification value for homogeneity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...
The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.