Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,614 recalls have been distributed to Idaho in the last 12 months.
Showing 1641–1660 of 27,833 recalls
Recalled Item: Prestige Coil System /UDI-DI codes: PRES0153CXPPLT 00810068567311...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima Coil System /UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Valeda Light Delivery System Product Name: Light Based Recalled...
The Issue: U.S. customers were shipped devices that were configured for the European...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer C11137 Recalled by Beckman Coulter,...
The Issue: Analyzer has calibration issues where curves switched from passed to failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name:...
The Issue: Electrode placement labels on the Digital Acquisition Box (DAB) were applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SmartRelease ESTR (Endoscopic soft tissue release system)...
The Issue: Potential that the blade can unintentionally cut tissue prior to the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800WF Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800W Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800F Infusion System. Intended to provide intravenous infusion of...
The Issue: Unreleased software versions were installed on distributed devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: Soltive...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Potential for thermal incident including an unexpected occurrence of smoke,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity 4 Birthing Bed Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential for improper crimps on the signal wires of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PhenoMATRIX Recalled by Copan WASP Due to AI-powered bacterial culture plate...
The Issue: AI-powered bacterial culture plate interpretation and workup software does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....
The Issue: All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V Recalled...
The Issue: Recent post-market surveillance data suggests a possible association of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G7 iOS Application Recalled by Dexcom, Inc. Due to A bug in the 2.7.0...
The Issue: A bug in the 2.7.0 version of the G7 iOS App can cause the app to enter a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL CultureSwab EZ Collection and Transport System Recalled by Copan...
The Issue: Swabs for specimen collection may be prone to breakage during product usage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.