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. 1,076 recalls have been distributed to New York in the last 12 months.
Showing 26461–26480 of 55,896 recalls
Recalled Item: Bauer's Candies Caramels NET WT 4 oz (bag) & bulk Recalled by Bauer's...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 8 oz assorted modjeska/chocolate modjeskas Recalled by Bauer's Candies, Inc....
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Modjeskas Bauer's Candies NET WT 8 oz Recalled by Bauer's Candies, Inc. Due...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sea Salt Bauer's Candies Modjeskas NET WT 8 oz bag Recalled by Bauer's...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1 lb QVC combo Recalled by Bauer's Candies, Inc. Due to Risk of Hepatitis A...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk assorted Recalled by Bauer's Candies, Inc. Due to Risk of Hepatitis A...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pentax Medical C2 CryoBalloon Standard 90 degree Catheter Recalled by PENTAX...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Recalled by Philips Medical Systems Nederlands Due to...
The Issue: During automatic tabletop movement, pressing and holding the Stop Table...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Pear Focal Catheter Recalled by PENTAX of...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Standard Focal Catheter Recalled by PENTAX of...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC Recalled by...
The Issue: Potential for fluorescein interference to cause inaccurately elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Visitec Soft Tip Cannula Recalled by Beaver Visitec Due to Certain lots...
The Issue: Certain lots are missing a protective sheath component over the silicone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion lnterventional Fluoroscopic X-ray System Recalled by Philips Medical...
The Issue: Philips has discovered through customer complaints and internal testing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.