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 2166121680 of 46,762 recalls

DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Penicillin G 100 Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Testosterone Cypionate 250 mg/mL Sterile Injection Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Tri-Mix 8.33:22.5:0.833 Injection Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Polyhexamethylene Biguanide 0.02% Ophthalmic Drops Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Phenylephrine 1 mg/mL Injection Recalled by Anderson Compounding Pharmacy,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: HCG 20 Day Extra Strength Recalled by Anderson Compounding Pharmacy, Inc....

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Quad-Mix 20:30:1:0.15 Injection Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Phenol 10% Injection Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Tri-Mix 50:30:1 Recalled by Anderson Compounding Pharmacy,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...

The Issue: There is a potential for the single use suction valve to come apart and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Incorrect part description contained on an additional label placed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Dornier Medtech America, Inc.

Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...

The Issue: Pin hole package failures compromising sterility of product

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

Class II — Potential Health HazardOngoing
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Dairy & Corn Free Bread Mix 19oz Recalled by Wholesome...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Banana Bread Mix 14oz Recalled by Wholesome Treats, Inc....

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Classic Herb Bread Mix 19oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund