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. 1,913 recalls have been distributed to New York in the last 12 months.
Showing 34361–34380 of 55,896 recalls
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...
The Issue: Product sterility is compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing, LLC Due to...
The Issue: The main vial label lists the incorrect part number, but the cap label is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...
The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics notified customers that errors were contained in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...
The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Parmesan Truffle Salt. The product is packaged in glass taster Recalled by...
The Issue: Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by G & W Laboratories,...
The Issue: CGMP Deviations: an expired active ingredient was used in the manufacture of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 20x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 17x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx50cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx40cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx50cm right Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker Visum¿ LED Surgical Lighting system is intended to Recalled by...
The Issue: The potential hazard that can arise for the combination of the missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.