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.
Showing 2061–2080 of 27,512 recalls
Recalled Item: Proxima Drape labeled as FACE LIFT. Sterile surgical drape. Recalled by...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Endotracheal Tube Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: Affected devices have a smaller diameter than expected and may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel BLOOD AGAR EMB AGAR BIPLATE Recalled by Remel, Inc Due to Potential...
The Issue: Product may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel BLOOD AGAR MacCONKEY AGAR BIPLATE Recalled by Remel, Inc Due to...
The Issue: Product may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: 1) MTS Recalled by MEDLINE INDUSTRIES, LP...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: PML Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: MTS Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z1 Femoral Hip System Recalled by Zimmer, Inc. Due to There is a potential...
The Issue: There is a potential design issue with the Z1 Offset Stem Inserter leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) AV FISTULA PACK-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.