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. 2,258 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,258 in last 12 months

Showing 4388143900 of 46,762 recalls

Medical DeviceMarch 6, 2013· Smith & Nephew Inc

Recalled Item: TRIGEN (TM) L-P SCREW Recalled by Smith & Nephew Inc Due to One batch of 4.5...

The Issue: One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner. Used...

The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner....

The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....

The Issue: The recall was initiated because Alere San Diego has an update for the Alere...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Carefusion Corporation

Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...

The Issue: The recall was initiated because Carefusion has received reports of a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 6, 2013· Carefusion Corporation

Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...

The Issue: The recall was initiated because Carefusion has identified potential risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2013· Kimberly-Clark Corporation

Recalled Item: KIMGUARD Container Filters Recalled by Kimberly-Clark Corporation Due to...

The Issue: Some individual container filter units might contain thin areas that may...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2013· Zydus Pharmaceuticals USA Inc

Recalled Item: Venlafaxine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...

The Issue: Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2013· Stryker Endoscopy

Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...

The Issue: In certain operating room environments, a colored screen image occurs with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2013· Stryker Endoscopy

Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...

The Issue: In certain operating room environments, a colored screen image occurs with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2013· Stryker Endoscopy

Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...

The Issue: In certain operating room environments, a colored screen image occurs with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2013· Philips Healthcare Inc.

Recalled Item: Philips IntellVue Info Center iX 866023 Recalled by Philips Healthcare Inc....

The Issue: If a customer creates customized trend scales in the trend review tile and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2013· Biosense Webster, Inc.

Recalled Item: 20-Pole Eco Cable Recalled by Biosense Webster, Inc. Due to Biosense is...

The Issue: Biosense is recalling the 20-Pole Eco Cable because it was incorrectly...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2013· Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Recalled Item: Chicken of the Sea 5-Ounce Chunk Light Tuna in Oil. Recalled by Tri-Union...

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