Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,043 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,043 in last 12 months

Showing 11821–11840 of 47,938 recalls

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: 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· 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: 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: 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: 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: 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: 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: 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· 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
Medical DeviceMay 24, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283)...

The Issue: It may occur that after system startup no stand movement is possible any...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Tandem Diabetes Care Inc

Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...

The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with...

The Issue: The automated dispensing cabinet software update included a .dll file that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Tandem Diabetes Care Inc

Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...

The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...

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

Class II — Potential Health HazardOngoing
FoodMay 24, 2022· Fudgeamentals LLC

Recalled Item: PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS Recalled by...

The Issue: made with peanut butter contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 24, 2022· Calico Cottage Inc

Recalled Item: 1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer...

The Issue: Fudge contains peanut butter that is potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 24, 2022· Fudgeamentals LLC

Recalled Item: PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS Recalled by Fudgeamentals...

The Issue: made with peanut butter contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 24, 2022· Calico Cottage Inc

Recalled Item: 1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package...

The Issue: Fudge contains peanut butter that is potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 24, 2022· Fudgeamentals LLC

Recalled Item: Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ) Recalled by Fudgeamentals LLC...

The Issue: made with peanut butter contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund