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. 2,544 recalls have been distributed to Idaho in the last 12 months.
Showing 12801–12820 of 48,215 recalls
Recalled Item: Virus Counter Platform with Model Name VC3100 Recalled by Sartorius...
The Issue: The Virus Counter is an automated laboratory instrument that enables rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus 30 Priority Pack w/.096 RHV - WPL2122277-01 Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDEFLATOR Plus 30 - WPL2122277-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 INDEFLATOR - WPL2122268-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack Accessory Kit/.096 RHV - WPL2122270-01 Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack w/COPILOT - WPL2122272-01 (2019-03-01) Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Risedronate Sodium Tablets Recalled by Macleods Pharma Usa Inc Due to FAILED...
The Issue: FAILED CONTENT UNIFORMITY SPECIFICATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Item # 721-1000 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 744-4930 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 714-5000 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 721-0200 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 722-0105 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 714-0706 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 731-0120 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 744-4875 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 743-0278 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.