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.

46,762 total recalls
2,374 in last 12 months

Showing 2270122720 of 46,762 recalls

DrugOctober 5, 2018· Amerigen Pharmaceuticals Inc.

Recalled Item: Temozolomide capsules Recalled by Amerigen Pharmaceuticals Inc. Due to...

The Issue: Failed dissolution specifications: Out-of-Specification dissolution results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 5, 2018· LUPIN SOMERSET

Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 4, 2018· Callie's Charleston Biscuits

Recalled Item: Callie's Charleston Biscuits COUTRY HAM BISCUITS Recalled by Callie's...

The Issue: The firm was notified by one of their vendors that the ham used in their...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 4, 2018· Callie's Charleston Biscuits

Recalled Item: Callie's Charleston Biscuits COCKTAIL HAM BISCUITS Recalled by Callie's...

The Issue: The firm was notified by one of their vendors that the ham used in their...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 3, 2018· GE Medical Systems, LLC

Recalled Item: SIGNA Architect system Product Usage: The Signa Architect system is Recalled...

The Issue: A small area on the bore surface, which is normally accessible to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2018· Medtronic Inc.

Recalled Item: Medtronic MiniMed 630G 6025805-003_C Recalled by Medtronic Inc. Due to...

The Issue: Reports of occurrences in which insulin pumps with version 4.10 software...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Healthful Naturals DizziFree Oral Spray Recalled by Silver Star Brands Due...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2018· Pfizer Inc.

Recalled Item: Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL...

The Issue: Correct Labeled Product Mispack: confirmed report involving a single unit of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies VertiFree Oral Spray Recalled by Silver Star Brands Due to...

The Issue: Microbial Contamination of Non-Sterile Products

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Healthful Naturals Leg Cramp Support Oral Spray Recalled by Silver Star...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies VaricoGo Oral Spray Recalled by Silver Star Brands Due to...

The Issue: Microbial Contamination of Non-Sterile Products

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies HypoSlim Oral Spray Recalled by Silver Star Brands Due to...

The Issue: Microbial Contamination of Non-Sterile Products

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· Silver Star Brands

Recalled Item: Native Remedies EyeClear Pro Oral Spray Recalled by Silver Star Brands Due...

The Issue: Microbial Contamination of Non-Sterile Product

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 3, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: Amlodipine Besylate USP 10 mg Tablets Recalled by InvaGen Pharmaceuticals,...

The Issue: Subpotent Drug: One lot of product does not meet the product specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2018· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: Discoloration: Presence of dark discoloration or brown spots on the edges of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR CPNB Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/HR CPNB Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/H FH DL 30hole SAT C Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550x 0.5 7 ml/hr Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF550x5ML/H 2ML 60LO 6" CATH Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing