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. 2,348 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,348 in last 12 months

Showing 2466124680 of 27,254 recalls

Medical DeviceJuly 17, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Custom Perfusion System. Model Numbers: 1D80R8 Recalled by...

The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Atrium Medical Corporation

Recalled Item: PleuraGuide Disposable Chest Tube Kit Recalled by Atrium Medical Corporation...

The Issue: Individual component's IFUs are not included with the kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Assuramed

Recalled Item: Hemoccult II BRAND SENSA elite Recalled by Assuramed Due to The products may...

The Issue: The products may have been stored at temperatures outside their required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Assuramed

Recalled Item: ProTime Microcoagulation System Recalled by Assuramed Due to The products...

The Issue: The products may have been stored at temperatures outside their required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Assuramed

Recalled Item: DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid...

The Issue: The products may have been stored at temperatures outside their required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Zimmer, Inc.

Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer recently conducted a review of historic packaging validations...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Aesculap, Inc.

Recalled Item: UNITRAC Pneumatic Retraction Arm. A support arm used to hold Recalled by...

The Issue: Changes were implemented to the UNITRAC instructions for use to ensure safe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· HemoCue AB

Recalled Item: HemoCue¿ Urine Albumin Microcuvettes Recalled by HemoCue AB Due to HemoCue...

The Issue: HemoCue AB has become aware of a production related problem involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards EndoReturn Arterial Cannula Recalled by Edwards Lifesciences, LLC...

The Issue: Edwards Lifesciences is recalling certain lots of the EndoReturn Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT and Brilliance iCT SP These systems are intended Recalled by...

The Issue: An artifact that resembles thrombus may appear on the image.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials International) Recalled...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (50 Count International Catalog Number:...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials Canada) Recalled by Nova...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (10 Count Boxed) Catalog Number: Recalled by...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (50 Count Retail) Catalog Number: Recalled by...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (10 Count Vials) Catalog Number: Recalled by...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (50 Count DME) Catalog Number: Recalled by Nova...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· HemoCue AB

Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by HemoCue AB Due to During a...

The Issue: During a complaint investigation HemoCue AB discovered punctured HemoCue...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (100 Count Retail Canada)Catalog Number:...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal Insufflation Tubing sets: 1) Insufflation Tubing Recalled by DeRoyal...

The Issue: DeRoyal Industries is recalling their product Insufflation Tubing Sets due...

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

Class II — Potential Health HazardOngoing