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. 1,763 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,763 in last 12 months

Showing 3498135000 of 48,215 recalls

Medical DeviceNovember 18, 2015· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...

The Issue: The treatment table positioning belt can slip gear positions, resulting in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...

The Issue: Potential post-processing software issue when using tabcard "4D" on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Biomet, Inc.

Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...

The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Zimmer Biomet, Inc.

Recalled Item: Zimmer Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet is initiating a...

The Issue: Zimmer Biomet is initiating a recall of the Virage Occipital Eyelet, as it...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...

The Issue: Some tubes were manufactured with the stopper not fully inserted into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...

The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 16, 2015· The Kroger Co

Recalled Item: BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS:...

The Issue: The firm was notified by a consumer of undeclared walnuts in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 16, 2015· Novarad Corporation

Recalled Item: NovaPACS  Diagnostic Viewer versions 8.3.7 Recalled by Novarad Corporation...

The Issue: The SUV values that are being calculated in the PET/CT fusion tool are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Smith & Nephew, Inc.

Recalled Item: BIRMINGHAM HIP RESURFACING MODULAR HEAD Recalled by Smith & Nephew, Inc. Due...

The Issue: The 16 devices distributed in the United States were incorrectly labeled as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: DrugSmart Cup 10 Recalled by Ameditech Inc Due to Ameditechs Drugs of Abuse...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: 11 Panel Card (OPI 300) w/Adult Recalled by Ameditech Inc Due to Ameditechs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ImmuTest Cup 7-panel w/ Adulteration Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen CLIA Waived Cup with 6 Drugs Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: Immutest 12 Panel Cup w/Adulteration Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: Immutest 10 Pnl Drug Screen Cup w/ Adult Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing