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. 1,837 recalls have been distributed to New York in the last 12 months.
Showing 39881–39900 of 55,896 recalls
Recalled Item: Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by...
The Issue: Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fabi-Saa Mote Blanco Net Wt. 14 oz. (397 g) Imported Recalled by FABI - SAA...
The Issue: Fabi-Saa Mote Blanco contains undeclared sulfites at 2.61 mg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED Recalled by...
The Issue: Twinings English Breakfast Black Tea 12ct Kcups, were packaged in cartons...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...
The Issue: There were two potential interference conditions identified with the way the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Inspection Technologies Recalled by GE Inspection Technologies, LP Due to...
The Issue: GE Inspection Technologies, LP ("GE") has discovered that certain of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...
The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...
The Issue: The door latch may not fully close and the door may open unexpectedly. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipogems SPA Aspiration Cannulae Recalled by Globalmed Logistix Due to The...
The Issue: The cannulae may bend during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...
The Issue: On a rare occasion, there is a potential to assign a patient result to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triple Ginger Brew Recalled by Trader Joes Company Due to Trader Joes...
The Issue: Trader Joes recalling Triple Ginger Brew due to reports of unopened bottles...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lindane Lotion Recalled by Morton Grove Pharmaceuticals, Inc. Due to...
The Issue: Super-Potent Drug: Out of Specification Assay test results were reported for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XCEL Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared Fluoxetine
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Confirmed customer compliants of finding an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.