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 2184121860 of 46,762 recalls

DrugMarch 11, 2019· Teva Pharmaceuticals USA

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Teva...

The Issue: Subpotent Drug.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 11, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...

The Issue: One of the software algorithms used to detect sample dispense errors was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Brainlab AG

Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...

The Issue: There is a potential for an incorrect dose distribution calculation by...

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2019· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium USP Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP deviation: Product found to contain trace amounts of NMBA

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2019· Hometown Food Company

Recalled Item: Pillsbury Unbleached All Purpose Flour Enriched 5Lb paper bag retail....

The Issue: Product may be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades:Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Blades Monopolar Recalled by Gyrus ACMI, Inc. Due to Olympus...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Malleable Recalled by Gyrus ACMI, Inc. Due to Olympus Diego...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Olympus Diego Elite Console MDCONS 100 Recalled by Gyrus ACMI, Inc. Due to...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
DrugMarch 7, 2019· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Mirapex (pramipexole dihydrochloride) Tablets Recalled by Boehringer...

The Issue: Failed Tablet/Capsule Specifications: identification of low weight tablets...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2019· Medtech Products, Inc.

Recalled Item: Little Remedies New Baby Essentials Kit. Each kit contains 1 Recalled by...

The Issue: Incorrect/undeclared excipients: Kit carton bear incorrect labeling for two...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 7, 2019· GOOD KARMA FOODS INC

Recalled Item: PL Trader Joe Natural Creamer - Vanilla 12/32oz Recalled by GOOD KARMA FOODS...

The Issue: Product was recalled due to undeclared milk. The Contains statement does not...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing