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. 2,333 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,333 in last 12 months

Showing 3240132420 of 46,762 recalls

Medical DeviceMarch 22, 2016· Coloplast Manufacturing US, LLC

Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...

The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....

The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Stryker Neurovascular

Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...

The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Stryker Neurovascular

Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...

The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...

The Issue: The affected scanner does not correctly interact with the SC360 software....

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2016· Hospira Inc.

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Hospira Inc. Due to Presence...

The Issue: Presence of Particulate Matter: particulate matter identified as an insect...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 18, 2016· NOW Foods

Recalled Item: Gingko Biloba 60mg packaged in a white and orange bottle Recalled by NOW...

The Issue: Undeclared soy lecithin in 5 dietary supplements.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 18, 2016· NOW Foods

Recalled Item: Goldenseal Root 500 mg packaged in a white and orange Recalled by NOW Foods...

The Issue: Undeclared soy lecithin in 5 dietary supplements.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 18, 2016· NOW Foods

Recalled Item: Elderberry 500 mg packaged in a white and orange bottle Recalled by NOW...

The Issue: Undeclared soy lecithin in 5 dietary supplements.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 18, 2016· NOW Foods

Recalled Item: Cranberry extract packaged in a white and orange bottle containing Recalled...

The Issue: Undeclared soy lecithin in 5 dietary supplements.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 18, 2016· NOW Foods

Recalled Item: Andrographis extract 400 mg packaged in a white and orange Recalled by NOW...

The Issue: Undeclared soy lecithin in 5 dietary supplements.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2016· Becton Dickinson & Company

Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...

The Issue: The device may have a defect in the catheter. In some instances this defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...

The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...

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

Class II — Potential Health HazardOngoing
DrugMarch 17, 2016· Impax Laboratories, Inc.

Recalled Item: Fenofibrate Capsules (Micronized) 134 mg Recalled by Impax Laboratories,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2016· Impax Laboratories, Inc.

Recalled Item: Fenofibrate Capsules (Micronized) 200 mg Recalled by Impax Laboratories,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
FoodMarch 17, 2016· Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Recalled Item: Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Oil Recalled by...

The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...

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

Class II — Potential Health HazardOngoing
Refund