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. 2,503 recalls have been distributed to Alaska in the last 12 months.
Showing 12321–12340 of 46,762 recalls
Recalled Item: TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Dissolution Specifications; during long term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable Recalled by Drug...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable Recalled by Drug Depot,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Dissolution Specifications; during long term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/ANASTROZOLE *GS* OIL 200MG/1MG/ML Injectable Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: (CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc.,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...
The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Lap Chole Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS IR - Angio Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inactivated macrolide-resistant Mycoplasma genitalium Recalled by...
The Issue: The QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYMJEPI (epinephrine injection Recalled by Adamis Pharmaceuticals...
The Issue: Defective Delivery System: Potential clogging of the needle preventing the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...
The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.