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. 1,834 recalls have been distributed to New York in the last 12 months.
Showing 46101–46120 of 55,896 recalls
Recalled Item: Black Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...
The Issue: An investigation identified that high level friction may exist between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Post-op Surgical Kits Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Wound Dressing Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Daily Dressing Packets Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...
The Issue: These microcatheters were packaged with a 2.8 F distal tip, rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Saturated Gauze Dressing Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Calibrator E Recalled by Siemens Healthcare Diagnostics, Inc Due to...
The Issue: Positive bias for Calibrator E lot kits ending in 38 and 39 with the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilling Knife Handles: a) b) c) Recalled by Teleflex Medical Due to The...
The Issue: The knife handles slot depth is out of specification, so blades may not fit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Presence of split or broken tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Sun Pharma...
The Issue: Failed Dissolution Specifications; 12 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specification; at the 6-month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pillsbury Biscuit Flaky Layers retail 4pk package. Recalled by General...
The Issue: Undeclared Milk ingredient on retail package. In error, individually wrapped...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cases of Pillsbury Biscuits Buttermilk 4pk. (6 - 4pk / case) Recalled by...
The Issue: Undeclared Milk ingredient on retail package. In error, individually wrapped...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Recalled by...
The Issue: The insulin pump may lose time and date settings during a power interruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equate Moisture Last Multi-Purpose Solution Recalled by Bausch & Lomb Inc-...
The Issue: Product lot did not meet the specification for its disinfectants at the time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with the following systems: Philips Allura Xper Systems...
The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...
The Issue: Loss of key image functionality due to a bent pedal of the Footswitch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety...
The Issue: An investigation identified that the product was incorrectly manufactured as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed...
The Issue: The Easy-Care Care-Lock feature installed at the foot of the bed may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: siemens Dimension¿ Phenytoin Flex¿ Reagent Cartridge The PTN method used...
The Issue: Internal testing has confirmed a low absorbance range between the levels 1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.