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. 999 recalls have been distributed to New York in the last 12 months.
Showing 46841–46860 of 55,896 recalls
Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...
The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS Recalled by Aesculap, Inc. Due...
The Issue: Aesculap Inc. (AIC (USA)) has initiated a voluntary recall of Dafilon Black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriceRite Spring Water Net 1 GAL (3.78 L) Distributed by Recalled by...
The Issue: Spring Water was found to be positive for E. Coli bacteria.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vita Classic Premium Sliced Smoked Atlantic Nova Salmon Recalled by Vita...
The Issue: This voluntary recall is being initiated due to a positive Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Colors
The Issue: Undeclared colors Blue #1, Blue #2 and Red #40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shoprite Spring Water Net 1 GAL (120 Fl Oz.) 3.78L Recalled by Readington...
The Issue: Spring Water was found to be positive for E. Coli bacteria.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Color
The Issue: Undeclared color Red #3 .
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Colors
The Issue: Undeclared colors Blue #1, Red #3 and Yellow #5.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Titan T 5K Motor Product Usage: Low-speed motor is used Recalled by Dental...
The Issue: The housing of 5K motor was laser marked incorrectly as a 20K motor. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...
The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Laceration Kit Recalled by Medical Action Industries Inc Due to Some...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Set Recalled by Medical Action Industries Inc Due to Some of the...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P...
The Issue: A small number of sealed foil pouches containing the electrodes were found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...
The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Medi-Pak Recalled by Medical Action Industries Inc Due to Some of...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port-A-Cath Tray Recalled by Medical Action Industries Inc Due to Some of...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.