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. 2,283 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,283 in last 12 months

Showing 4198142000 of 46,762 recalls

Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Quick Thin (citrus aurantium extract Recalled by Bethel Nutritional...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Bethel Advance (bitter orange Recalled by Bethel Nutritional Consulting, Inc...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company/3m Espe Dental Products

Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...

The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Medicel Ag

Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...

The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2013· American Health Packaging

Recalled Item: Valacyclovir HCl Tablets Recalled by American Health Packaging Due to Subpotent

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2013· Dr. Reddy's Laboratories, Inc.

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

The Issue: Microbial Contamination of Non-Sterile Products: A lot of raw material used...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2013· CTV Best Group

Recalled Item: BEST Slim Recalled by CTV Best Group Due to Undeclared Drug

The Issue: Marketed without an Approved NDA/ANDA: Product contains an undeclared drug,...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 1, 2013· Nexus Pharmaceuticals Inc

Recalled Item: Benztropine Mesylate Injection Recalled by Nexus Pharmaceuticals Inc Due to...

The Issue: Presence of particulate matter: characterized as thin colorless flakes that...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2013· AbbVie Inc.

Recalled Item: Mavik¿ trandolapril tablets 4mg Recalled by AbbVie Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Package Insert; product packaged with outdated version...

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

Class III — Low RiskOngoing
Refund
FoodAugust 1, 2013· Gourmet Express Marketing, Inc.

Recalled Item: Breaded Recalled by Gourmet Express Marketing, Inc. Due to Packages of...

The Issue: Packages of breaded shrimp failed to declare shellfish (shrimp) and wheat...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 1, 2013· Superior Nut Co. Inc.

Recalled Item: Raw Pistachio Halves Recalled by Superior Nut Co. Inc. Due to Potential...

The Issue: Positive laboratory result for Salmonella sp. Speciation in progress.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 1, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...

The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Nidek Inc

Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...

The Issue: Under certain circumstances, the Left eye image may be saved as the Right...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Zimmer, Inc.

Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...

The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...

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

Class II — Potential Health HazardOngoing