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 1441–1460 of 27,833 recalls
Recalled Item: Preat Recalled by Preat Corp Due to Due to manufacturing error, digital...
The Issue: Due to manufacturing error, digital analog rotational feature is 180 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Recalled by Thoratec...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number:...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to A...
The Issue: A potential issue with the Automated Impella Controller (AIC) not detecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical...
The Issue: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical...
The Issue: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR System Software. Model Number: 444829. Recalled by Becton Dickinson &...
The Issue: Potential for functionality issue that supports the Over labeling feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Nellcor Bedside SpO2 Patient Monitoring System: Recalled by...
The Issue: Bedside SpO2 Patient Monitoring System alarms not heard/recognized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinia Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varicam Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated...
The Issue: Foley catheter may have an obstructed lumen, which may result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant...
The Issue: There is the potential that the silicone implant may contain foreign material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Patient Connector Recalled by Medtronic, Inc....
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...
The Issue: Dipstick strep A test has potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...
The Issue: Due to an incorrect test results provided that indicated the incorrect drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabFlush Prefilled Syringe with ICU Medical SwabCaps Recalled by MEDLINE...
The Issue: SwabFlush syringes are affected by the ICU Medical recall of their SwabCap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PhaSeal Injector Luer (N30C) Recalled by BD SWITZERLAND SARL Due to...
The Issue: Closed system drug transfer devices were shipped to the U.S. market without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.