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. 2,245 recalls have been distributed to Alaska in the last 12 months.
Showing 46101–46120 of 46,762 recalls
Recalled Item: The product is Pathfinder SL Recalled by Spacelabs Healthcare, Llc Due to...
The Issue: The firm received reports of the Pathfinder LS software crashing after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dent's Extra Strength Toothache Gum Recalled by Grandpa Brands Co Due to...
The Issue: Superpotent; benzocaine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The product has the Catalogue/Part number 60010. Olympic Cool-Cap System...
The Issue: The Olympic Cool-Cap's Control Module has experienced a frozen screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand name: RayStation. Generic name: Treatment Planning System. Software...
The Issue: The firm decided to recall when an issue was found with the dose calculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED TRANSPLANT PACK Product Usage: The Sarns Cardioplegia Cannula and...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FX PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 12-GAUGE...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.