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. 2,336 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,336 in last 12 months

Showing 3106131080 of 46,762 recalls

Medical DeviceJuly 14, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...

The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Diasorin Inc.

Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...

The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2016· Supernus Pharmaceuticals, Inc.

Recalled Item: Trokendi XR (topiramate) extended-release capsule Recalled by Supernus...

The Issue: Superpotent Drug: Failure of assay specifications in the capsule.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2016· McCain Foods USA

Recalled Item: Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta...

The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2016· McCain Foods USA

Recalled Item: Fire roasted Poblano & Jalapeno popper bites packaged in a Recalled by...

The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2016· ELITech Group B.V.

Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...

The Issue: Software malfunction; The action being taken due to the device becoming...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2016· Mckesson Medical Imaging Group

Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...

The Issue: The STAT priority icon was not displayed in the Study List when the study...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2016· Resmed Corporation

Recalled Item: Quattro Air FFM MED  AMER Recalled by Resmed Corporation Due to Masks in...

The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...

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

Class II — Potential Health HazardOngoing
DrugJuly 11, 2016· Actavis Inc

Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis Inc...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· HVL, LLC

Recalled Item: ULTRA PROTEIN VANILLA¿ 948 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· HVL, LLC

Recalled Item: METABOLIC CLEANSE REVISED 1181 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· HVL, LLC

Recalled Item: METABOLIC CLEASNSE VEG 1151 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED Recalled by Bausch & Lomb Inc...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....

The Issue: The product lot failed to meet QC acceptance criteria during stability...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing