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 2698127000 of 27,254 recalls

Medical DeviceOctober 28, 2011· Shimadzu Medical Systems

Recalled Item: 0.7/1.3U163CS-36 In combination with below systems MobileArt Evolution...

The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2011· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to As part of GE Innova IQ...

The Issue: As part of GE Innova IQ table introduction, a label was designed to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2011· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Liquid Creatine Kinase Reagent Set Device is a Recalled by...

The Issue: Linear performance information in product insert does not match that listed...

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

Class III — Low RiskOngoing
Medical DeviceOctober 19, 2011· Merge Healthcare, Inc.

Recalled Item: CADstream software Product Usage: CADstream is an image processing system...

The Issue: Customers may experience an issue with the software study preferences when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2011· Philips Healthcare Inc.

Recalled Item: Philips Healthcare Practix Convenio Mobile X-ray system Worldwide...

The Issue: When the system is switched off or when the tube arm is parked in the down...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2011· Exactech, Inc.

Recalled Item: OPTETRAK LOGIC Proximal Tibial Spacer & Screws (2) 2.5 LT BLUE Size 2.5...

The Issue: Exactech, Inc. of Gainesville, FL recalled their Optetrak Proximal Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2011· SCC Soft Computer

Recalled Item: SoftLab with SA INST versions: 3.1.6.12 Recalled by SCC Soft Computer Due to...

The Issue: On 10/17/2011 SCC Soft Computer, Clearwater, FL initiated a correction on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2011· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Surgical System IS3000 with the da Vinci Recalled by Intuitive...

The Issue: Improper restraints during transportation of the da Vinci system could cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Intuitive Surgical, Inc.

Recalled Item: Thyroidectomy Indication for the da Vinci Surgical Systems Recalled by...

The Issue: Promotional literature for use of the da Vinci system for thyroidectomy,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxI 600 Access Immunoassay Systems Recalled by Beckman Coulter Inc....

The Issue: The recall was initiated because Beckman Coulter has received seven reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxC 660i Recalled by Beckman Coulter Inc. Due to The recall was...

The Issue: The recall was initiated because Beckman Coulter has received seven reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxI 800 Access Immunoassay Systems Recalled by Beckman Coulter Inc....

The Issue: The recall was initiated because Beckman Coulter has received seven reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2011· Beckman Coulter Inc.

Recalled Item: Access Total T3 Reagent Recalled by Beckman Coulter Inc. Due to A recall was...

The Issue: A recall was initiated because Beckman Coulter has identified a negative...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-4975 HSG Tray containing 4 oz. bottle PVP Prep Solution Recalled by...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-4873 Custom CT Biopsy Tray Recalled by Custom Medical Specialties, Inc....

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-8450-R1 Custom Vein Tray containing 4 oz. bottle PVP Prep Recalled by...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-4316 Custom Vein Tray containing 4 oz. bottle PVP Prep Recalled by...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-2586 Custom Amnio Tray containing 2 oz. bottle PVP Prep Recalled by...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-8457 Hysteroscopic Sterilization Pack containing 4 oz. bottle PVP Prep...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: BR980-9600 Hysteroscopy Sterile Procedure Kit containing 2 oz. bottle PVP...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing