Product Recalls in Alaska
Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 950 recalls have been distributed to Alaska in the last 12 months.
Showing 30241–30260 of 46,762 recalls
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: 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: 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: 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: 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: 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 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: 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: 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: 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: OPEN HEART KIT WITH 03ML FLUSH DEVICE FOR FLETCHER ALLEN HEALTH CARE...
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: The surgical table is a stand alone unit. Three (3) Recalled by Schaerer...
The Issue: The floor locking cylinders contained in the base of the Schaerer 7300 model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche COBAS INTEGRA c111 Analyzer Recalled by Roche Diagnostics Operations,...
The Issue: cobas c 111 analyzers (catalog numbers 04777433001 and 04528778001) with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heater Cooler Unit Usage: The Heater-Cooler Unit (HCU 30) supplies Recalled...
The Issue: There is the potential for contaminated water to enter parts of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIPLE (3) DISPOSABLE TRANSDUCER KIT WITH 03ML FLUSH DEVICE FOR 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: ART LINE KIT W/ 3ML FLUSH DEVICE FOR JACKSON MEM. HOSP. 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: Cath Lab Kit w/3 Port "ON" Manifold (600 psi) Recalled by 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: TRANSPAC¿ IV MONITORING KIT Recalled by ICU Medical, Inc. Due to 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.