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. 1,027 recalls have been distributed to Alaska in the last 12 months.
Showing 15721–15740 of 46,762 recalls
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.
Recalled Item: Lab Coats SMS Medium White 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.
Recalled Item: Phytonadione Tablets 5mg Recalled by Bausch Health Companies, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mephyton (phytonadione) Tablets 5mg Recalled by Bausch Health Companies,...
The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by American...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 23G 4MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 25G 4MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-200H-8022 22G EZSHOT ASPIRATION NEEDLE Recalled by Aomori Olympus Co.,...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-204 GUIDE SHEATH KIT 2.6MM 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.
Recalled Item: B5-2Q BALLOON CATHETER 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.
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.
Recalled Item: NA-401D-1321 ASPIRATION NEEDLE 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.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 23G 6MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.