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. 2,510 recalls have been distributed to North Dakota in the last 12 months.
Showing 11301–11320 of 27,512 recalls
Recalled Item: 8" (20 cm) Appx 0.33 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 78 IN (198cm) APPX 10.0 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 123 IN (312cm) APPX 16.1 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURPLUG Nano Connector.1 unit per pouch Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 124" (315 cm) 60 Drop 150 mL Burette Set (w/Clave Recalled by ICU Medical,...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 148 IN (376cm) APPX 18.8 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112 IN (284cm) APPX 14.8ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 54 IN (137 cm) APPX 7.2 ml EXT SET w NanoClave 4-Way Stopcock Recalled by...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5" (14 cm) Appx 0.39 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11 IN(28cm)APPX 0.97ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112 IN(284cm) APPX 14.6ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.32 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 IN (25cm) APPX 1.5ml EXT w/6-Port NanoClave Manifold Recalled by ICU...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 128" (325 cm) Appx 16.6 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedics 6.0MM ROD Recalled by OrthoPediatrics Corp Due to Product may...
The Issue: Product may have incorrect laser etched alignment lines, the non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.