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. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1572115740 of 46,762 recalls

Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Isolation W/Ties Univ Ylw Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Lab Coats SMS 2X-Large Blue Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Kendall Blue XXL Recalled by Cardinal Health 200, LLC Due to Foreign...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Kendall Blue L Recalled by Cardinal Health 200, LLC Due to Foreign...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Becton Dickinson & Co.

Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System Catalog number (REF) Recalled by...

The Issue: Some N1 and N2 master mix pouches packaged within the lots of BioGX...

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

Class II — Potential Health HazardOngoing
DrugJanuary 6, 2021· DLC Laboratories, Inc

Recalled Item: Sulfur Ointment 10% Recalled by DLC Laboratories, Inc Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2021· Respironics California, LLC

Recalled Item: PHILIPS BATTERY Recalled by Respironics California, LLC Due to Due to...

The Issue: Due to unqualified "design verification" batteries being shipped to customers.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2021· Baxter Healthcare Corporation

Recalled Item: Infusion Pump Recalled by Baxter Healthcare Corporation Due to Battery...

The Issue: Battery performance issues related to prolonged storage.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: 9180 Electrolyte Analyzer - Product Usage: intended to be used Recalled by...

The Issue: May display Calcium results on the screen with wrong arrow direction which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2021· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for Recalled by Arrow...

The Issue: The lidstock / information card on the kits correctly states the product...

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

Class II — Potential Health HazardOngoing
FoodJanuary 5, 2021· Dole Fresh Vegetables Inc

Recalled Item: Dole Chopped Kit Sesame Asian Salad & Topping Net Wt: Recalled by Dole Fresh...

The Issue: Incorrect product master-pack label causing an undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2021· Helena Laboratories, Corp.

Recalled Item: Cascade Abrazo aPTT Test Card - Product Usage: are to Recalled by Helena...

The Issue: Intermittent potential for shorter than expected clot times.

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

Class II — Potential Health HazardOngoing
DrugJanuary 4, 2021· Nostrum Laboratories Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2021· Ittella International, LLC

Recalled Item: Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life...

The Issue: A gluten free claim was inadvertently used on the lid of the container....

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX 25G 2.5MM Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: KD-611L ELECTROSURGICAL KNIFE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: K-202 GUIDE SHEATH KIT 2.0MM Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 3MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: SD-230U-20 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: PR-V614M 2-LUMEN CANNULA Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing