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. 2,311 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,311 in last 12 months

Showing 3680136820 of 46,762 recalls

FoodMarch 3, 2015· Stonewall Kitchen, LLC

Recalled Item: Stonewall Kitchen Buffalo Wing Sauce Net Wt. 17.5 oz. glass Recalled by...

The Issue: Undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 3, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2015· American Health Packaging

Recalled Item: Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 2, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: The FLOW-i Anesthesia System Axillary O2 and Suction Module Recalled by...

The Issue: Maquet has identified that in some FLOW-i Anesthesia System Auxiliary O2 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2015· Hill-Rom, Inc.

Recalled Item: Steriseal-Cannula Ophthalmic Recalled by Hill-Rom, Inc. Due to The metal...

The Issue: The metal cannula attached to the handpiece can rotate and become dislodged...

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

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2015· Akorn, Inc.

Recalled Item: Fluticasone Propionate Nasal Spray Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Stability Specifications: Out of specification for preservative,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
FoodFebruary 27, 2015· Unilever United States, Inc.

Recalled Item: Talenti Gelato & Sorbetto Recalled by Unilever United States, Inc. Due to...

The Issue: Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Stryker received four customer complaints reporting that inside the box...

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 26, 2015· Ethicon Endo-Surgery Inc

Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...

The Issue: During an internal inspection of the production process the firm discovered...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...

The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Quest Medical, Inc.

Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...

The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...

The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...

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

Class II — Potential Health HazardOngoing
Refund