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. 2,551 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,551 in last 12 months

Showing 1196111980 of 48,215 recalls

Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. McKesson Rapid Test Kit McKesson Consult Fertility Test hCG Recalled by...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Palmero Healthcare Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Alere Toxicology TABLET Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. McKesson DISINFECTANT Recalled by Mckesson Medical-Surgical Inc....

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Recalled by Mckesson...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Dynarex¿ PAD Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MERIT MEDICAL SYSTEMS Temno Soft Tissue Biopsy Device Temno 14 Recalled by...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: COOPER SURGICAL Milex PESSARY Recalled by Mckesson Medical-Surgical Inc....

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Mckesson GYNECATH H/S CATHETER 5FR (10/CS) Model Number: 11-19610 Recalled...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MEDLINE INDUSTRIES Medline Catheter Insertion Tray Medline Foley Without...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Fischer Cone Biopsy Excisor EXCISOR Recalled by Mckesson Medical-Surgical...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: 3M COMPANY 3M PAD Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MORRISON MEDICAL Morrison Medical OB KIT Recalled by Mckesson...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Dynarex SWAB Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Cook Incorporated

Recalled Item: Pressure Monitoring Set Recalled by Cook Incorporated Due to The products...

The Issue: The products may contain excess coating material on the outside and/or...

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

Class II — Potential Health HazardOngoing
DrugMay 24, 2022· Grato Holdings, Inc.

Recalled Item: Homeopathic EarAche Drops Recalled by Grato Holdings, Inc. Due to Microbial...

The Issue: Microbial contamination of non-sterile product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri Ajo King con Ortiga y Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund