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. 2,487 recalls have been distributed to Alaska in the last 12 months.
Showing 12541–12560 of 46,762 recalls
Recalled Item: Excelsior Medical 10mL Sterile Field Saline Flush ZR Recalled by MEDLINE...
The Issue: Sterility failure of the exterior of the syringe which may impact the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VESSEL SEALER EXTEND Recalled by Intuitive Surgical, Inc. Due to Placing...
The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi' Recalled by Intuitive...
The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 2) UPN: M00542421 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 1) UPN: M00542420 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 1) UPN:M0054242CE0 Intended Use:...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Aid Kits containing acetaminophen under brand names Equate (Walmart)...
The Issue: Kits contained recalled acetaminophen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Delivery Catheter System. Part of the Harmony Transcatheter...
The Issue: There is potential for the capsule bond to break during the procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars...
The Issue: Undeclared allergen - egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AccessPLUS Large Bore Hemostasis Valves Recalled by Merit Medical Systems,...
The Issue: A design change made to a hemostasis valve to improve manufacturability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access-9 Large Bore Hemostasis Valves Recalled by Merit Medical Systems,...
The Issue: A design change made to a hemostasis valve to improve manufacturability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORE-SIGHT ELITE Absolute Tissue Oximeter Recalled by Edwards Lifesciences,...
The Issue: The StO2 values may be inaccurately low when using either the FORE-SIGHT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORE-SIGHT ELITE Tissue Oximeter module Recalled by Edwards Lifesciences,...
The Issue: The StO2 values may be inaccurately low when using either the FORE-SIGHT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.