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 2222122240 of 46,762 recalls

Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera 1.5T High Performance Recalled by Philips Medical Systems Nederlands...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 20, 2018· Akorn Inc

Recalled Item: COSOPT Ophthalmic Solution Recalled by Akorn Inc Due to Failed Stability...

The Issue: Failed Stability Specifications: out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 20, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 20, 2018· Funky Chunky LLC

Recalled Item: Nutty Choco Pop Recalled by Funky Chunky LLC Due to Nutty Choco Pop has in...

The Issue: Nutty Choco Pop has in incorrect label and does not declare that it contains...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 20, 2018· Merge Healthcare, Inc.

Recalled Item: The WinStation Retinal Imager Recalled by Merge Healthcare, Inc. Due to...

The Issue: Certain configurations of Merge Eye Station hardware may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...

The Issue: When switching back & forth between multiple UV instances in the Windows...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· TERRIFIC CARE LLC

Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...

The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...

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

Class I — Serious Health HazardOngoing
DrugDecember 19, 2018· Teva Pharmaceuticals USA

Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 19, 2018· Associates of Cape Cod, Inc.

Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...

The Issue: The kits may contain the incorrect number of components or the kits may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing