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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 14181–14200 of 46,762 recalls
Recalled Item: BD Gravity Burette Set 60 DP 3 SmartSite VALVES BALL VALVE DRIP CHAMBER...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SmartSite Bag Access Device Needle-Free Valve Recalled by CAREFUSION Due...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Infusion Buerette Set Smallbore Tubing Smartsite Port...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Extension Set SMALLBORE Tubing SmartSite VALVE Recalled by CAREFUSION Due...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD ADD-ON Burette Set V/NV Needle-Free Valve Recalled by CAREFUSION Due to...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steripath Luer Transport Pack Recalled by Magnolia Medical Technologies,...
The Issue: Product was shipped with the incorrect Transfer Adapter Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLUDARABINE PHOSPHATE FOR INJECTION Recalled by Custopharm, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: the manufacturing firm had microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg...
The Issue: Failed Stability Specifications; out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.25 mg...
The Issue: Failed Stability Specifications; out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phantom Nail System Recalled by Paragon 28, Inc. Due to A thin wall...
The Issue: A thin wall condition between the inner cannulation and the flutes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Ready-To-Use Primary Antibody CDX2 (EP25) Recalled by Leica...
The Issue: Product may not perform as specified in IFU.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arjo Disposable Repositioning Sling Recalled by Getinge Dominican Republic...
The Issue: Sling loop straps on device pose a trip hazard.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia CX 3.0T-Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated...
The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.