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. 949 recalls have been distributed to Arkansas in the last 12 months.
Showing 40281–40300 of 49,990 recalls
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp Due to...
The Issue: Presence of Particulate Matter: Confirmed customer complaints received for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops A.C. (Tetrahydrozoline HCl 0.05% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops Advanced Relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops (Tetrahydrozoline HCl 0.05%) Recalled by K C Pharmaceuticals Inc...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops Industrial Strength (Polyethylene glycol 400 1% Recalled by K C...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...
The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...
The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...
The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...
The Issue: Failed Stability Specifications: Product is subpotent and has out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotoprone Therapy System. The Rotoprone Therapy System is an advanced...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWEREASE Instruments Set Screw Breakoff Instrument Recalled by Medtronic...
The Issue: The retaining tabs component of the Set Screw Retaining Drive may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...
The Issue: Suboptimal routing of the cable may result in increased wear over time....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.