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. 902 recalls have been distributed to North Dakota in the last 12 months.
Showing 46881–46900 of 47,938 recalls
Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...
The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...
The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Campbell's Oyster Stew Recalled by Campbell Soup Supply Co., LLC Due to The...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PathFinder NXT Pivoting Percutaneous Rod Holder This device is an Recalled...
The Issue: Complaints have been reported where, during surgery, the surgeon was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The carton label for...
The Issue: The carton label for this device has the manufacturer symbol where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The Tyvek pouch...
The Issue: The Tyvek pouch label for this device states: 'with holster'; however, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M525 F50 Surgical Microscope Recalled by Leica Microsystems, Inc. Due...
The Issue: Leica Microsystems evaluated data showing that a malfunction resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap(R) - Miethke Shunt System Recalled by Aesculap, Inc. Due to The...
The Issue: The deflector may not move freely on the ventricular catheter. The deflector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trizivir (abacavir sulfate 300mg Recalled by GlaxoSmithKline Inc Due to...
The Issue: Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg tables, Lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Product is a liquid dietary supplement packaged in white plastic Recalled by...
The Issue: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clams Recalled by Rhee Brothers Incorporated Due to Frozen clams, product of...
The Issue: Frozen clams, product of S. Korea, may be contaminated with Norovirus.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...
The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4-Hytrel Zipper Toga Product Usage - The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.