Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 989 recalls have been distributed to Nebraska in the last 12 months.
Showing 31741–31760 of 49,150 recalls
Recalled Item: Gildess 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical, Inc....
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess 24 FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advance Trauma Kit - Product Code 85-0742 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: USCG Boat Response Kit - Product Code 80-0353 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Range Trauma Kit ORG - Product Code 80-0213 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amphibious Trauma Kit - Product Code 85-0639 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Range Trauma Kit - Product Code 85-1274 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: K-9 Trauma Field Kit - Product Code 80-0211 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mini Resupply Trauma Kit - Product Code 85-0835 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc. Due...
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gildess FE 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc....
The Issue: Subpotent Drug; Ethinyl Estradiol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aid Backpack Kit - Product Code 85-0917 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neonate Kit With 30 ml Flush Device For Driscoll Foundation For Children...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC CVL MONITORING KIT W/03ML FLUSH DEVICE FOR YALE NEW HAVEN HOSP....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONITORING KIT W/03ML FLUSH DEVICE FOR MEDICAL COLLEGE OF GA Recalled by ICU...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 PORT "OFF" MANIFOLD Recalled by ICU Medical, Inc. Due to ICU Medical Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Catheterization Right Heart Kit w/2-Station Recalled by ICU Medical,...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSDUCER KIT WITH 03ML FLUSH DEVICE FOR ALL CHILDRENS HOSP. Recalled by...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIFURCATED DISPOSABLE TRANSDUCER KIT W/03ML FLUSH DEVICE FOR JOHNS...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.