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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 15361–15380 of 46,762 recalls
Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing...
The Issue: Microbial Contamination of Non-Sterile Products: firm's internal testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizer...
The Issue: CGMP Deviations: lots recalled due to CGMP deviations because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing...
The Issue: CGMP Deviations: lots recalled due to CGMP deviations because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizer...
The Issue: Microbial Contamination of Non-Sterile Products: firm's internal testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Remel Haemophilus Test Medium(100mm) 10/PK Recalled by Remel Inc Due to When...
The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium (150 mm) 10/PK Recalled by Remel Inc Due to...
The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio X.pree Recalled by Siemens Medical Solutions USA, Inc Due to A patient...
The Issue: A patient image was assigned to a different patient during image recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics SafeSheath ULTRALITE 10F Recalled by Oscor, Inc. Due to...
The Issue: Potential for open seal on sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE Irrigation Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of particulate matter.one confirmed customer report of particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A610 Clinician Programmer Application for Deep Brain Stimulation Clinician...
The Issue: There are two issues within this correction action: 1. Cycling Issue: When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Live Better vegan vitamin d-3 by CVS Health Recalled by New Generation...
The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VEGAN VITAMIN D3 Recalled by New Generation Wellness Inc. Due to Vitamin D3...
The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 VR-T Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 VR-T DX Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.