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 2656126580 of 27,254 recalls

Medical DeviceJune 14, 2012· Integra Life Sci.

Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...

The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2012· Philips Healthcare Inc.

Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...

The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...

The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Teleflex Medical

Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...

The Issue: Speaker Failure. If the speaker fails and an event occurs which would...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Carestream Health, Inc.

Recalled Item: Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health...

The Issue: Carestream DRX-1 System batteries manufactured before June 2012 due to two...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware through complaints of a potential safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2012· Tedan Surgical Innovations Llc

Recalled Item: Sterile Distraction Screws of 3 different sizes: 12mm Recalled by Tedan...

The Issue: This letter is to notify you that several of our sterile screw products are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Merit Medical Systems, Inc.

Recalled Item: Custom Procedural Trays: Merit's Custom Total Hip Pack Recalled by Merit...

The Issue: Custom Procedural trays contain Stryker Hytrel Togas which are being...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune Rover Waste Management System Recalled by Stryker Instruments Div....

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Neptune Bronze Rover Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 1 Silver Rover Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2012· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Slice CT Scanner System is a computed Tomography X-ray...

The Issue: One of the four screws that secure the Oil-accumulator to the X-Ray Tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 1 Gold Rover (120 Vand 230V ) Waste Management Recalled by Stryker...

The Issue: Stryker has received two reports of serious injury as a result of tissue...

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

Class I — Serious Health HazardOngoing