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. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1476114780 of 46,762 recalls

DrugMay 11, 2021· DIBAR NUTRICIONAL S DE RL DE CV

Recalled Item: DiBAR LABS Hand Sanitizer Recalled by DIBAR NUTRICIONAL S DE RL DE CV Due to...

The Issue: CGMP Deviations: Other lots and products of hand sanitizer recalled because...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2021· DASH XCLUSIVE

Recalled Item: Imperia Elita Vitaccino Coffee Recalled by DASH XCLUSIVE Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis determined presence of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2021· Exactech, Inc.

Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....

The Issue: The HAT trial contains a retaining ring that has shown the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Skytron, Div. The KMW Group, Inc

Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...

The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Randox Laboratories Ltd.

Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...

The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· IMPLANTCAST GMBH

Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...

The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Ventec Life Systems, Inc.

Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...

The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· BioFire Diagnostics, LLC

Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...

The Issue: Elevated rates of false negative results may occur when using blood culture...

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

Class II — Potential Health HazardOngoing
DrugMay 7, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...

The Issue: Subpotent and Presence of Particulates .

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

Class III — Low RiskOngoing
Refund
FoodMay 7, 2021· Slayer Forever, LLC dba BUBS Naturals

Recalled Item: BUBS Naturals MCT OIL Powder Recalled by Slayer Forever, LLC dba BUBS...

The Issue: Firm was notified by supplier of Medium Chain Triglycerides (MCT) that it...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 7, 2021· SARA LEE FROZEN FOODS

Recalled Item: Sara Lee Pecan Pie 4oz. retail packaged Recalled by SARA LEE FROZEN FOODS...

The Issue: Potentially undeclared peanut

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 7, 2021· Magellan Diagnostics, Inc.

Recalled Item: LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098 Recalled by...

The Issue: Magellan has received reports that control tests of either the Low-Control...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2021· Magellan Diagnostics, Inc.

Recalled Item: LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004 Recalled by...

The Issue: Magellan has received reports that control tests of either the Low-Control...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2021· Magellan Diagnostics, Inc.

Recalled Item: LeadCare II Blood Lead Test Kit Catalog Number 70-6762 Recalled by Magellan...

The Issue: Magellan has received reports that control tests of either the Low-Control...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2021· K2M, Inc

Recalled Item: Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2...

The Issue: Mislabeled product labeling incorrect length or height, or length and height...

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

Class II — Potential Health HazardOngoing