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. 2,245 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,245 in last 12 months

Showing 4628146300 of 46,762 recalls

DrugApril 9, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ciprofloxacin Tablets Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 9, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC...

The Issue: ConMed Linvatec is recalling the product due to the punch being...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2012· Gulf Fiberoptics, Inc.

Recalled Item: GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink. GMF-RC65...

The Issue: The GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink falls...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Steris Corporation

Recalled Item: STERIS 5085 and 5085 SRT Surgical Tables Recalled by Steris Corporation Due...

The Issue: STERIS has learned from Customer feedback and field service experience that...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Etac Supply Center Ab

Recalled Item: Etac¿ Ono Walker Recalled by Etac Supply Center Ab Due to The recall has...

The Issue: The recall has been initiated because there is the potential that users may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2012· Invacare Corporation

Recalled Item: TDX SP Power Wheelchair Recalled by Invacare Corporation Due to Invacare...

The Issue: Invacare Corporation decided to recall the product because of a potential...

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

Class II — Potential Health HazardOngoing
DrugApril 5, 2012· Apotex Corp.

Recalled Item: Meloxicam Tablets Recalled by Apotex Corp. Due to Tablet Thickness: Recall...

The Issue: Tablet Thickness: Recall was initiated due to the presence of one slightly...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2012· Hospira, Inc.

Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira, Inc. Due to...

The Issue: Superpotent (Single Ingredient) Drug: Above specification assay results for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 4, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima Mobile X-ray System. The GE Automatic Mobile Recalled...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
FoodApril 3, 2012· Deep Foods Inc

Recalled Item: Crispy by TWI Foods Pistachio Cookies Recalled by Deep Foods Inc Due to...

The Issue: Products may contain undeclared milkand almonds.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2012· Deep Foods Inc

Recalled Item: Crispy by TWI Foods Coconut Cookies Recalled by Deep Foods Inc Due to...

The Issue: Products may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2012· Deep Foods Inc

Recalled Item: Crispy by TWI Foods Almond Cake Rusk Recalled by Deep Foods Inc Due to...

The Issue: Products may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 3, 2012· Deep Foods Inc

Recalled Item: Crispy by TWI Foods Almond Cookies Recalled by Deep Foods Inc Due to...

The Issue: Products may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 3, 2012· Beckman Coulter Inc.

Recalled Item: Unicel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the UniCel DxH 800 Coulter Cellular Analysis...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2012· Ethicon, Inc.

Recalled Item: Ethicon Surgiflo Hemostatic Matrix Kit with Thrombin Plus Flex Tip Recalled...

The Issue: The lyophilized thrombin component of the Surgiflo Hemostatic Matrix kit...

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

Class II — Potential Health HazardOngoing
DrugApril 2, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Mefloquine HCL Tablets Recalled by Teva Pharmaceuticals USA, Inc. Due to...

The Issue: Tablet Thickness: Product is being recalled due to the potential of being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 2, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Restoration Modular Cone Body Trials Stryker Ireland...

The Issue: Stryker Orthopaedics has become aware of a burr, or a metal shaving,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2012· Hill-Rom, Inc.

Recalled Item: Affinity Four Birthing Bed P3700 Product Usage: The Affinity Recalled by...

The Issue: During review of our last braking system via that field corrective action,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2012· Greiner Bio-One North America, Inc.

Recalled Item: Vacuette Quickshield Complete Plus Recalled by Greiner Bio-One North...

The Issue: : The Quickshield Complete Plus may have a defect (split at the base), which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2012· Medical Components, Inc dba MedComp

Recalled Item: MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Recalled...

The Issue: Product was packaged with the incorrect port and does not match the label....

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

Class II — Potential Health HazardOngoing