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. 2,374 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,374 in last 12 months

Showing 1988119900 of 27,254 recalls

Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing