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. 2,659 recalls have been distributed to New York in the last 12 months.
Showing 28561–28580 of 55,896 recalls
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A nonsterile bulk product designated for further processing in a tray was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Earthrise Natural Spirulina Recalled by Earthrise Nutritionals Llc Due to...
The Issue: The product may contain small metal pieces (approximately 2 mm to 8 mm) from...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...
The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc...
The Issue: Incorrect Product Formulation: wrong sunscreen product in the package.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Admelog Solostar (insulin lispro injection) Recalled by Sanofi-Aventis U.S....
The Issue: Temperature Abuse: Product samples of Admelog may not have been shipped at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities and Degradation Specifications and Subpotent Drug:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by Medgyn Products, Inc. Due...
The Issue: CGMP Deviations: The manufacturer of this product recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...
The Issue: Incorrect expiration being entered for one lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...
The Issue: The analyzer software may cause a mis-match of patient demographics and test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...
The Issue: One lot of product is from product code AK-22502 so it contains a 2-lumen, 5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...
The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection USP 3.375 grams per vial Recalled...
The Issue: Presence of Particulate Matter: identified as glass and silicone material
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Product: ABL800 FLEX with Crea. The ABL800 with Crea is Recalled by...
The Issue: From three incidents in Denmark and Sweden, comparison studies on patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.