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. 2,573 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,573 in last 12 months

Showing 31413160 of 47,938 recalls

FoodJanuary 22, 2025· La Fiesta Food Products

Recalled Item: La Fiesta PAN RAYADO Bread Crumbs Recalled by La Fiesta Food Products Due to...

The Issue: Firm distributed a Bread Crumb product with undeclared allergen (Sesame) not...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 22, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· Provepharm Inc.

Recalled Item: Phenylephrine HCl Injection Recalled by Provepharm Inc. Due to Presence of...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 21, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· AvKARE

Recalled Item: Irbesartan Tablets USP Recalled by AvKARE Due to Out of Specification for...

The Issue: Out of Specification for Dissolution

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate Recalled by...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX--MEDIAL TIBIA PLATE 12H RT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate Recalled by...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing