Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,083 recalls have been distributed to Oklahoma in the last 12 months.
Showing 11481–11500 of 28,654 recalls
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.
Recalled Item: Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (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: 004550004 GTIN: 14026704663085 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product...
The Issue: Insufficient amount of antibody without an error message or alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 0.82 ml Recalled by ICU Medical, Inc. Due to Identification of a...
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: 13 IN (33cm) APPX 0.96 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: 13 IN(33cm) APPX 1.0 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: 7" (18cm) Appx 0.31 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: 6.5" (17 cm) Appx 0.35 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: 7 IN (18CM) APPX 0.26ml 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: 114" (290 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....
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: 26 IN(66cm) APPX 3.9 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: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....
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 0.29 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: DISTALE - 203 cm (80") Bifuse Ext Set w/6 Gang 1o2 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: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...
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: 6" (15 cm) Appx 0.26 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.