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. 2,619 recalls have been distributed to New York in the last 12 months.
Showing 34901–34920 of 55,896 recalls
Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...
The Issue: Products were made outside of Quality System Regulation, and potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: The company received a customer complaint for the inability to calibrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra...
The Issue: There is a possibility for data to be stored under the wrong patient on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 25 mg Recalled by InnovaGel Due to Subpotent
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dye Free Allergy Softgel Gelatin Capsule Recalled by InnovaGel Due to Subpotent
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alfuzosin Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Presence of Foreign Substance: consumer complaint for foreign matter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cappuccino Snack Mix Lot code: 20161027 Recalled by Dutch Valley Food...
The Issue: As a result of an ingredient supplier recall, Dutch Valley is issuing a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ADVIA Centaur Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Total Knee System Vanguard Open Box Femoral Components Item...
The Issue: packaging of some femoral components was incorrectly labeled as either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.