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. 2,026 recalls have been distributed to New York in the last 12 months.
Showing 18621–18640 of 55,896 recalls
Recalled Item: INJECTOR FORCEMAX UP 2MM CH 25G 4MM Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2MM CH 23G 6MM Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-V243Q-A 3-LUMEN EXTRACTION BALLOON V Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 25G 5MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRESCENT SNARE Recalled by Aomori Olympus Co., Ltd. Due to Inspection...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-411D-1521 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-210U-10 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 26G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 23G 5MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-201SX-4021 ASPIRATION NEEDLE VIZISHOT 21G Recalled by Aomori Olympus Co.,...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to...
The Issue: Product distributed with a red tape as part of the sterile packaging which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse USP 0.12% Recalled by Precision Dose Inc....
The Issue: cGMP deviations: The firm was notified of the manufacturer's expanded recall.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection 1 Recalled by AuroMedics Pharma LLC Due to...
The Issue: Discoloration and failed pH specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz Recalled by...
The Issue: Labeling: Missing instructions for use insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...
The Issue: The Quality Control (QC) card has a label error for the standard deviation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "Divvies Vegan and Nut Free Vanilla Cupcakes with Vanilla Frosting Recalled...
The Issue: Cupcakes contain undeclared milk and egg due to supplier ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tegral Satin EC CL Vegan Cake packaged in 50lbs bags Recalled by Puratos...
The Issue: Undeclared milk and egg in cake flour
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Divvies Vegan and Nut Free Vanilla Cupcakes with Chocolate Frosting...
The Issue: Cupcakes contain undeclared milk and egg due to supplier ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.