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. 1,032 recalls have been distributed to North Dakota in the last 12 months.
Showing 15341–15360 of 47,938 recalls
Recalled Item: Medtronic CB7J98R7 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic BB10R94R6 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8M63R4 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8R62R13 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB1H18R20 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10Y89R10 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10W64R1 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 1A46R11 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10W63R1 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrostatic Filter Angled Recalled by Covidien, LP Due to The company was...
The Issue: The company was notified by their supplier of sterilization services for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10W65R1 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic BB11J14R2 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY10D90R2 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox RX Imola Analyser with ISE Recalled by Randox Laboratories Ltd. Due...
The Issue: An issue was identified where the software froze during processing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II...
The Issue: Incorrect stentstop assembly (18fr) was used to build the delivery system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW 4x6 Acidophilus Recalled by NOW Health Group Inc. Due to Undeclared...
The Issue: Foreign capsules included in bottle. Undeclared ingredients.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...
The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride 0.9% Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DELFELX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...
The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DELFLEX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...
The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.