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. 2,317 recalls have been distributed to Alaska in the last 12 months.
Showing 35761–35780 of 46,762 recalls
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Praeger's California Veggie Burgers Gluten Free 11 oz. Manufactured...
The Issue: Dr. Praeger's Gluten Free California Burgers contain undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...
The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon PS X3 Tibial Insert Recalled by Stryker Howmedica Osteonics Corp....
The Issue: Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PowerLED / X-TEN / VOLISTA Surgical Light Systems are Recalled by Maquet...
The Issue: Maquet Suspension Arms used with PowerLED/X-TEN/Volista Surgical Light...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System software RayStation is a...
The Issue: An error caused by a floating point precision problem tends to cause a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nice! Powdered Sugar Mini Donuts 11.5 oz packaged in a Recalled by Walgreen...
The Issue: Nice! Powdered Sugar Mini Donuts may contain mold. Alleged illnesses have...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril maleate and hydrochlorothiazide tablets USP Recalled by Apotex...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Innova IGS 540. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 630. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 620. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 740 & GE Healthcare Innova IGS Recalled by GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730. Angiographic X-ray systems used in Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 3100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.