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. 2,535 recalls have been distributed to North Dakota in the last 12 months.
Showing 7461–7480 of 27,512 recalls
Recalled Item: Endo Stitch V-Loc 180 Absorbable Reload Recalled by Covidien, LP Due to...
The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Stitch V-Loc PBT Non-Absorbable Reload Recalled by Covidien, LP Due to...
The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Reusable Gel Pack Recalled by Cardinal Health 200, LLC Due...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Guide X-Mark Probe Tool -used for registering edentulous patients to...
The Issue: Product missing one of two welds connecting the tip to the shaft, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zio AT Clinical Manual Recalled by iRhythm Technologies, Inc. Due to...
The Issue: Ambulatory ECG monitoring system labeling update: 1) Clinically actionable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 9X10X10mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Hammertoe Continuous Compression Implants Recalled by Synthes...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...
The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #:...
The Issue: Assigned vial lot numbers for the incorrect type of product. SARS-CoV-2 &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C6 Recalled by Hamilton Medical AG Due to Due to a malfunction...
The Issue: Due to a malfunction related to the backlight on the ventilator screen. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...
The Issue: Due to increase in Li-Ion Battery failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.