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. 2,673 recalls have been distributed to New York in the last 12 months.
Showing 24461–24480 of 30,153 recalls
Recalled Item: Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Athrosurface 40mm 13.75x31mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Myoglobin Calibrator (MYO CAL) Recalled by Siemens...
The Issue: Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE Recalled by Express...
The Issue: This recall has been initiated due to potential false positives results when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial One Lumen Tube - Right Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Right) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheopart Set (Right) Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White Bronchial Double Lumen Tube Set (Right) Sterile Recalled by Teleflex,...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheopart Set (Left) Recalled by Teleflex, Inc. Due to Customer complaints...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device 20G x1 Recalled by Smiths Medical...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryogenic probe for cardiac ablation surgery Recalled by Atricure Inc Due to...
The Issue: Affected product may have compromised sterility due to packaging defects. It...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Port A Cul tubes with Swabs Sterile Pack Recalled by Becton Dickinson &...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Port A Cul tubes Recalled by Becton Dickinson & Co. Due to The products...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL PT-Fibrinogen HS PLUS Recalled by Instrumentation Laboratory Co. Due...
The Issue: Some vials of HemosIL PT-Fibrinogen HS PLUS, Part No. 0008469810 (various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / Recalled...
The Issue: Accuray has become aware of a potential safety issue related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.