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 2598126000 of 27,254 recalls

Medical DeviceOctober 30, 2012· Philips Healthcare Inc.

Recalled Item: Philips Digital Diagnost Software Version R2.0.2 Product Usage: This system...

The Issue: With Digital Diagnost R2.0.2 a mirrored "R in a circle" is burnt into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2012· Cordis Corporation

Recalled Item: Cordis Recalled by Cordis Corporation Due to Affected lots of Cordis ExoSeal...

The Issue: Affected lots of Cordis ExoSeal (TM) VCD have been sterilized using a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2012· iwalk inc

Recalled Item: BiOM Rechargeable Li Ion 22.2 V Battery and BiOM Lithium Recalled by iwalk...

The Issue: Battery may over-heat during charging and smoke

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2012· Hospira Inc.

Recalled Item: Plum A+ Single Channel Infusion Pumps with Hospira Mednet Software Recalled...

The Issue: The volume control knob on some Plum A+ single channel infusers (located on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2012· The Anspach Effort, Inc.

Recalled Item: Multiples Anspach Micro Curved Attachments (MCA) and Curved Burr Support...

The Issue: During a recent review of documentation Anspach determined that the current...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2012· Hospira Inc.

Recalled Item: Plum A+ Hyperbaric Single Channel Infusion Pumps with Hospira MedNet...

The Issue: The volume control knob on some Plum A+ single channel infusers (located on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2012· Hospira Inc.

Recalled Item: Plum A+ Single Channel Infusion Pumps with Plug-and-Play Modules that...

The Issue: The volume control knob on some Plum A+ single channel infusers (located on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2012· Beckman Coulter Inc.

Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the AU8500 Clinical Chemistry Analyzer because...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Quasar MD is an infrared LED lamp that is labeled Recalled by Quasar...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Baby Quasar (LAB-001-D Recalled by Quasar Bio-Tech, Inc. dba Silver Bay LLC...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Philips Healthcare Inc.

Recalled Item: Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers...

The Issue: When the operator for a wall stand view selects an "image rotation"...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Kerr Corporation

Recalled Item: BioPlant Recalled by Kerr Corporation Due to The firm initiated the recall...

The Issue: The firm initiated the recall becaue disturbing the BioPlant product soon...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Verathon, Inc.

Recalled Item: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that...

The Issue: Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Quasar Power Pack contains a Baby Quasar and a Baby Recalled by Quasar...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge.115mmx115mm Pledget Recalled...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing