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. 2,299 recalls have been distributed to Alaska in the last 12 months.
Showing 40701–40720 of 46,762 recalls
Recalled Item: Anspach Carbide Cutting Burrs: 2MM Carbide Fluted Ball Recalled by The...
The Issue: Some carbide cutting burr fractured during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Carbide Cutting Burrs & Drums: 1.5MM x 7.5MM Cylindrical Recalled by...
The Issue: Some carbide cutting burr fractured during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part #...
The Issue: Some carbide cutting burr fractured during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Carbide Cutting Burrs & Drums: 2MM Carbide Fluted Ball Recalled by...
The Issue: Some carbide cutting burr fractured during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VoLumen Barium Sulfate Suspension (0.1 % w/v Recalled by Bracco Diagnostics...
The Issue: Failed Stability Testing: This product is below specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine Hydrochloride Syrup (Cetirizine Hydrochloride Oral Solution...
The Issue: Failed impurities/degradation specifications; out of specification for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Artis zee Ceiling Systems. Angiographic x-ray system. Recalled by...
The Issue: During the lifetime of Artis zee Ceiling systems, there is an increased wear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100S Sterilization System Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 50 Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...
The Issue: Covidien is conducting a voluntary field corrective action on Puritan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pyridostigmine Bromide Tablets USP Recalled by Corepharma LLC Due to Failed...
The Issue: Failed Dissolution Specification: Corepharma Inc. is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...
The Issue: Ensuring all customers have the tools to assist in verifying the setting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectible Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Glass defect located on the interior neck of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candy Sweet Spots Recalled by Bee International, Inc. Due to Undeclared Egg
The Issue: Bee International is recalling Sweet Spots Candy because it has undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: Sterility of medical devices intended for use in surgical procedures may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.