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. 1,173 recalls have been distributed to New York in the last 12 months.
Showing 8081–8100 of 30,153 recalls
Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN)RFPC-35-180 ORDER...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RFSPC-35-180...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-150...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System with Version 3.7.2 and below Recalled by...
The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPW-35-150...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System with Version 3.7.2 and below Recalled by...
The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-150...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-150...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power electronic box Recalled by Myolyn Inc. Due to Screws mounting an...
The Issue: Screws mounting an internal power supply may come loose during shipping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NuVasive MD Pulse III Multimodality System Pulse Software Recalled by...
The Issue: Due to an incorrect security key, customers were unable to connect to remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Recalled by...
The Issue: Negative bias with patient samples. The mean patient sample bias range from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System...
The Issue: Incorrect expiration date listed on the product labels. The expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) GE Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Inaccurate Distance and Area measurements with use of Global Stack viewport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal limb holders: (1) DeRoyal Limb Holder Recalled by DeRoyal Industries...
The Issue: The webbing strap was laced improperly through the teeth of the buckle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e801 Immunoassay Analyzer Recalled by Roche Diagnostics Operations,...
The Issue: Software issue resulting in signals and sample test results of Pre-Wash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Exacta-Mix 2400 compounding system Recalled by Baxter Healthcare...
The Issue: There is a potential for leaking valves on ports 1 to 4 in certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.