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 29901–29920 of 46,762 recalls
Recalled Item: CANNIBAL FEROX AMPED Recalled by Chaos and Pain Due to Product was analyzed...
The Issue: Product was analyzed and found to contain 1,3- dimethylbutylamine which was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Performance-LOAD Ambulance Cot Fastener Stretcher Recalled by Stryker...
The Issue: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEVOXYL(R) (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...
The Issue: Superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...
The Issue: Due to a customer experiencing complaints on bone fraction of assay not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...
The Issue: The device defect associated with this recall may result in HbA1c values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...
The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is Recalled by...
The Issue: BD is conducting a voluntary product recall of the BD Spinal Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENNIS ELBOW SUPPORT Recalled by DeRoyal Industries Inc Due to DeRoyal...
The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PNEUGEL(R) TENNIS ELBOW STRAP Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems...
The Issue: Firm received reports about "acquisition errors" and the deterioration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin for Oral suspension Recalled by West-Ward Pharmaceuticals Corp....
The Issue: Labeling: Label Error on Declared Strength: Some bottles miss a color coded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a Recalled...
The Issue: The firm failed to notify current customers of IFU update/warning. During a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: OOS results for known compound.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VOCO Futurabond M+ adhesive Recalled by Voco GmbH Due to Labeling mix-up:...
The Issue: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue where certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.