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.
Showing 22641–22660 of 46,762 recalls
Recalled Item: Moe's Southwest Vegetarian Breakfast Bowl 8oz. Frozen 8 Recalled by Request...
The Issue: The firm was notified by their supplier that ingredients used in their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gordon Choice / GFS Vegetable Egg & Cheese Frittata 60oz. Recalled by...
The Issue: The firm was notified by their supplier that ingredients used in their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jenny Craig Butternut Squash Ravioli 213g. Frozen 30 Recalled by Request...
The Issue: The firm was notified by their supplier that ingredients used in their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kashi Recalled by Request Foods Incorporated Due to Potential Salmonella...
The Issue: The firm was notified by their supplier that ingredients used in their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Beecher's Mariachi Mac & Cheese 20oz. Frozen 8 Recalled by Request Foods...
The Issue: The firm was notified by their supplier that ingredients used in their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medfusion¿ Model 4000 Syringe Infusion Pump Recalled by Smiths Medical ASD...
The Issue: Customers who utilize PharmGuard¿ Server Software (PGS) with Medfusion¿ 4000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro...
The Issue: Marketed Without an Approved NDA/ANDA: Undeclared Sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cidofovir injection 375 mg/mL (75 mg/mL) vial Injection Recalled by Heritage...
The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Tartrate Injection Recalled by Baxter Healthcare Corporation Due...
The Issue: Failed pH Specifications: Upward shift in the pH of the solution within the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zimmer Compress Devices and Instruments: Item Number/Item Description 178350...
The Issue: Correction to update the surgical technique for the Compress System. To make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE Recalled by Atrium Medical...
The Issue: This recall has been initiated in response to a seal defect found in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...
The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...
The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....
The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrOXYzine HYDROCHLORIDE SYRUP (HydrOXYzine Hydrochloride Oral Solution...
The Issue: CGMP Deviations: cleaning procedures during manufacturing caused out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...
The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...
The Issue: It was identified that the volume of air inside the mattress may expand in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...
The Issue: This recall has been initiated due to a software defect found in the Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.