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. 2,648 recalls have been distributed to New York in the last 12 months.
Showing 31021–31040 of 55,896 recalls
Recalled Item: Toma Celena Recalled by Cooperstown Cheese Company, LLC Due to Potential...
The Issue: Cheese may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Garlic and Black Peppercorns. All package sizes are subject Recalled...
The Issue: Cheese may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Garlic Cheddar Recalled by Cooperstown Cheese Company, LLC Due to...
The Issue: Cheese may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag Recalled by...
The Issue: Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merkts Port Wine Cheese Spread Recalled by Bel Brands USA Due to Bel Brands...
The Issue: Bel Brands USA is recalling Merkts Port Wine Cheese Spread after being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duloxetine Delayed-release Capsules USP Recalled by AVKARE Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: slightly elevated levels of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A1 Slim Recalled by Kiriko, LLC. Due to Undeclared Sibutramine
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: No.1 Faiza Beauty Cream Manufactured by: Poonia Brothers (Pak) Recalled by...
The Issue: Marketed Without an Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...
The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...
The Issue: While reviewing documentation for the next software release of the 2008T, an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...
The Issue: The firm received complaints that involved an unanticipated interaction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...
The Issue: The product has a non-conformity that may cause clips to mislead, jam or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...
The Issue: Firewall installed with Philips IntelliVue Information Center iX or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling
The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirus Drill 13mm diameter trauma instrument used for preparation of Recalled...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Shaft hip and anatomical shoulder instrument used for preparation...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iBalance(R) UKA Recalled by Arthrex, Inc. Due to Arthrex part number...
The Issue: Arthrex part number AR-501-UFLC, size 3, batch 10123297, has the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Famotodine has an out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.