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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 29941–29960 of 46,762 recalls
Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Flexible Shaft Recalled by Synthes (USA) Products LLC Due to...
The Issue: Non-conforming material used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy Recalled by Mevion...
The Issue: Completing Setup Without Program Move Complete Can Cause An Isocenter Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skinny Bee Diet capsules Recalled by Love My Tru Body Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: presence of undeclared sibutramine,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol...
The Issue: Failed Stability Specifications: Low Out of Specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simply Nature Organic Red Split Lentils Recalled by Aldi Inc Due to...
The Issue: Product may contain undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Simply Nature Organic Green Lentils Recalled by Aldi Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Life Rising TT Side Head Regulator Recalled by Life Rising Corp S Due to...
The Issue: High levels of lead discovered in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nabisco Oreo Fudge Creme Original Variety Recalled by Mondelez International...
The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nabisco Oreo Fudge Creme Mint Variety Recalled by Mondelez International Due...
The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage:...
The Issue: IBA is initiating this recall to address an issue identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S...
The Issue: A change in the calibration curve causing an increase in false prozone flags.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Circumcision Clamps with separate O-Ring Component: The device is...
The Issue: Aesculap has received complaints of excessive bleeding after use of Gomco...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...
The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....
The Issue: Breach in sterile barrier compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...
The Issue: Failed Dissolution Specifications: The firm was notified that there was a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.