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. 2,771 recalls have been distributed to New York in the last 12 months.
Showing 15861–15880 of 30,153 recalls
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...
The Issue: The device has an offset in the design that results in a reading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer with Cross Enterprise Display This impacts...
The Issue: Remote comparison studies displayed may be associated with the wrong...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray BeneVision Distributed Monitoring System (DMS) Recalled by Mindray...
The Issue: The firm has identified performance anomalies with the device caused when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...
The Issue: There is a potential to generate falsely elevated serum or plasma chloride...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...
The Issue: The reagent pack exhibits the potential for an increased frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241-S Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass ULTRA SYSTEM Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...
The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.