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 1081–1100 of 27,833 recalls
Recalled Item: Getinge 88-Series Washer- Disinfector. Model Number: 88-5. Recalled by...
The Issue: Potential for device to overheat during operation if the circulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter....
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sharesource Connectivity Platform for Use with Homechoice Claria Product...
The Issue: Vantive has identified a software defect within the Sharesource Claria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mMR. Model Number: 10433372. Recalled by Siemens Medical Solutions...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Prisma. Model Number: 10849582. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Verio. Model Number: 10276755. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Lumina (DE). Model Number: 11344916. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396 Recalled by...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Vida Fit. Model Number: 11410481. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Cima.X (DE). Model Number: 11647158. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Verio Dot Upgrade. Model Number: 10684334. Recalled by Siemens...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.