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. 1,065 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,065 in last 12 months

Showing 2861–2880 of 47,938 recalls

DrugFebruary 25, 2025· A-S Medication Solutions LLC

Recalled Item: METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG Recalled by A-S Medication...

The Issue: Presence of Foreign Tablets/Capsules.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Operating table column TS7500 MOBIUS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (MC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Stationary column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (SC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Otopore Cylinder Standard outer ear dressings Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Recalled by Baxter Healthcare Corporation Due to There...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Ex Firm 4cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Ex Firm 8cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 8cm fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 4cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid Plus (FC) Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Mobile column TruSystem 7500 U Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing