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. 2,374 recalls have been distributed to Alaska in the last 12 months.
Showing 22581–22600 of 46,762 recalls
Recalled Item: Testosterone 12.5mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone 25 mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 18mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone 200 mg/Anastrozole 20 mg pellet Recalled by Qualgen, LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-401 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-400 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-RFP-456 Recalled by NxStage Medical, Inc....
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard Wolf Bronchoscope Tubes Recalled by Richard Wolf GmbH Due to There...
The Issue: There is a potential deficiency of the TEXAS Bronchoscope Tube product. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-402 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS)...
The Issue: An intermittent failure which causes a blender initialization fault upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-403 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-406 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-404 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-RFP-454 Recalled by NxStage Medical, Inc....
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...
The Issue: software malfunction; It was found when a user performs radiography using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...
The Issue: Potential that gauze pads may not be fully sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PLEX Elite 9000 Recalled by Carl Zeiss Meditec, Inc. Due to Under...
The Issue: Under certain fault conditions, the existing design may expose the operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.