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. 2,487 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,487 in last 12 months

Showing 1150111520 of 27,254 recalls

Medical DeviceMay 7, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If an examination is interrupted when the InSpect Projection View (PV) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker 1 End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2020· Endologix, Inc.

Recalled Item: Ovation iX Abdominal Stent Graft Systems Recalled by Endologix, Inc. Due to...

The Issue: A material weakness adjacent to the polymer fill channel may become...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 5, 2020· Olympus Corporation of the Americas

Recalled Item: ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use...

The Issue: Products repaired with the incorrect service manual may be missing an O ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X35MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 4.5X45MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X55MM Recalled...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X50MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X45MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X60MM Recalled...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X40MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X55MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing