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. 2,299 recalls have been distributed to Alaska in the last 12 months.
Showing 38981–39000 of 46,762 recalls
Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...
The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...
The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...
The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....
The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...
The Issue: Reports of unexpected movement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZyGenerics ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Superpotent Drug: A complaint was reported by a pharmacist who stated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin for Injection USP Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurity/Degradation Specification; high out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Port Access Kit with MicroClave Clear Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAP Change Kit w/MicroClave Clear Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor...
The Issue: The firm became aware of a potential problem that was initiated by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cap Change Kit with MicroClave Clear Connector Recalled by ICU Medical, Inc....
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Split Cath III Trays Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProSol - sulfite-free (Amino Acid) Injection Recalled by Baxter Healthcare...
The Issue: Presence of Particulate Matter: identification of particulates in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CUBICIN (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter: Potential presence of glass particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.