Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,053 recalls have been distributed to Arkansas in the last 12 months.
Showing 14721–14740 of 49,990 recalls
Recalled Item: BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented Recalled by...
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 0.2 Micron Filter Smallbore Recalled by...
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: BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite 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: 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 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: 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 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 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: 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-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: 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: 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) 0.05/0.25 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: Erythromycin Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...
The Issue: Defective container: possibility for lack of seal integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cimetidine Hydrochloride Oral Solution 300 mg/5 mL Recalled by PAI Holdings,...
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.