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 2416124180 of 27,254 recalls

Medical DeviceOctober 28, 2013· Abbott Point Of Care Inc.

Recalled Item: Abbott i-STAT PT/INR cartridges Abbott Point of Care Inc. Recalled by Abbott...

The Issue: Abbott Point of Care Inc (APOC) has determined that i-Stat PT/INR cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Nephros Inc

Recalled Item: Nephros SafeSpout Manufacturer: Nephros Inc. 41 Grand Avenue Recalled by...

The Issue: Promotional materials for non-medical water filtration products were...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 28, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam line of gamma camera systems Used to detect or Recalled by Siemens...

The Issue: Reports of loose bolts in the detector support structure of Symbia and e.cam...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E is a multi-purpose SPECT system ideal for hospitals Recalled by...

The Issue: Reports of loose bolts in the detector support structure of Symbia and E.CAM...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Toshiba American Medical Systems Inc

Recalled Item: Titan 3T MRI System Recalled by Toshiba American Medical Systems Inc Due to...

The Issue: Toshiba America Medical Systems, Inc. is recalling due to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Synovis Surgical Innovations, Inc.

Recalled Item: Dura Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...

The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra Disposable Recalled by Integra LifeSciences Corp. d.b.a. Integra...

The Issue: Integra LifeSciences Corporation is recalling certain lots of Integra Kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Synovis Surgical Innovations, Inc.

Recalled Item: Vascu Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...

The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Nephros Inc

Recalled Item: Nephros Dual Stage Ultra Filter (DSU) Brochure Document 60-3003 Revisions: 0...

The Issue: Promotional materials for non-medical water filtration products were...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 28, 2013· Nephros Inc

Recalled Item: 1) Nephros SafeShower FH - 15 filters per box Recalled by Nephros Inc Due to...

The Issue: Promotional materials for non-medical water filtration products were...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: 1) Accolade II 127 Neck Angle Hip Stem Recalled by Stryker Howmedica...

The Issue: Stryker received a report from the field indicating that an Accolade II Hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of Recalled by Roche...

The Issue: There is a software synchronization issue with the ACCU-CHEK Combo system....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Civco Medical Instruments Inc

Recalled Item: Civco Belly Board Recalled by Civco Medical Instruments Inc Due to Scales...

The Issue: Scales adhered to the product may be misaligned from the zero such that one...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Civco Medical Instruments Inc

Recalled Item: Civco Belly Board MRI Recalled by Civco Medical Instruments Inc Due to...

The Issue: Scales adhered to the product may be misaligned from the zero such that one...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery NMCT 670 Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Biomet, Inc.

Recalled Item: Security (TM) Enclosed Carpal Tunnel System Blade ( Recalled by Biomet, Inc....

The Issue: Security Blades were manufactured oversized and potentially won't advance or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Anti-HBs Calibrators & VITROS Anti-HBs Reagent Packs Recalled by...

The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Hospira Inc.

Recalled Item: *** 1) List number 126970465 labeled in part: 12697-65 LifeShield Recalled...

The Issue: Several lots of the LifeShield Latex-Free HEMA Y-Type Blood Set IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2013· Nobel Biocare Usa Llc

Recalled Item: Osseocare Pro Console & Set Osseocare Pro Recalled by Nobel Biocare Usa Llc...

The Issue: The recall was initiated because there is a potential for malfunction of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2013· Kimberly-Clark Corporation

Recalled Item: Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD...

The Issue: Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7...

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

Class II — Potential Health HazardOngoing