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. 2,503 recalls have been distributed to Alaska in the last 12 months.
Showing 11501–11520 of 46,762 recalls
Recalled Item: Recalled by MEDLINE INDUSTRIES, LP - SPT Due to Kits contain leaking bottles...
The Issue: Kits contain leaking bottles of isopropyl alcohol
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience kits labeled as: a. MAJOR VASCULAR CDS Recalled by...
The Issue: Kits contain leaking bottles of isopropyl alcohol
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Medline Product Name: convenience kits labeled as: LAP Recalled...
The Issue: Kits contain leaking bottles of isopropyl alcohol
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits labeled as: a. MIDDLE EAR PACK-LF Recalled by...
The Issue: Kits contain leaking bottles of isopropyl alcohol
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: CGMP Deviations: Manufacturing deviations were reported due to an abnormal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olopatadine HCl Recalled by Akorn, Inc. Due to Failed impurity/degradation...
The Issue: Failed impurity/degradation specifications: Out of specification for 2-HMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: CGMP Deviations: lots made with same active pharmaceutical ingredient (API)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Tablet/Capsule Specification; oversized tablet found in a bottle
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Recalled...
The Issue: Salmonella. Product contains recalled Jif peanut butter as ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ambu VivaSight 2 DLT Recalled by Ambu Inc. Due to Firm has received...
The Issue: Firm has received complaints on the device concerning leak/rupture of either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Microcatheter product label on the carton is missing the microcatheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627 Recalled...
The Issue: Milk contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 710-5364 Recalled...
The Issue: Milk contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Service manuals for the CT Recalled by GE Healthcare, LLC Due to As a result...
The Issue: As a result of unclear guidance in the service manual, the table can drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YelloPort Elite Universal Seal. For use in laparoscopic procedures. Recalled...
The Issue: There is the potential that YelloPort Elite Universal Seals packaging may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 45LS Ventilator- intended to provide continuous or intermittent...
The Issue: A forced shutdown of one of the processors did not generate a watch dog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INFINITY Resect Guide for INBONE Talus Recalled by Wright Medical...
The Issue: The instrument is incorrectly color coded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...
The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...
The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...
The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.