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. 2,623 recalls have been distributed to Arkansas in the last 12 months.
Showing 8121–8140 of 49,990 recalls
Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...
The Issue: Sterility of device may be compromised due to breach of the chevron seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Recalled...
The Issue: CGMP deviation: product released prior to supplier approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...
The Issue: cGMP deviations: Batch was released prior to approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...
The Issue: cGMP deviations: Batch was released prior to approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Green Curry Paste (one ounce) 28g contained in Every Plate meal code 87...
The Issue: Product spoiled due to temperature abuse.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...
The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to...
The Issue: A bottle of Copaliner Solvent was inadvertently packaged into a box labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenition 70. The device is to be used in health Recalled by Philips Medical...
The Issue: Philips has become aware of the potential for unintended radiation exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cosmedent FlexiCup Composite Finishing & Polishing System Recalled by...
The Issue: Reports were received the elastomer cup material is crumbling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: For intraventricular indications mainly used for operations within the brain...
The Issue: Trocar manufactured with the shaft too long and does not meet manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visera Hysterovideoscope Olympus HYF Type V Recalled by Olympus Corporation...
The Issue: IFU labeling is being updated to revise EtO gas mixture and elimination of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHOROPTOR VRX DIGITAL SYSTEM-Digital intended for the subjective Recalled by...
The Issue: Phoroptor VRx Head may detach from the bracket that connects the Phoroptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to...
The Issue: Replacement of the internal Sample Pump due to high failure rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom Boom models series: F110 Recalled by IHB OPERATIONS B.V. Due to...
The Issue: Weakened connection point on the adjustable suspension arm, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper series Recalled by Philips Medical Systems Nederland B.V. Due to...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion Recalled by Philips Medical Systems Nederland B.V. Due to A foot...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost-Eleva Recalled by Philips Medical Systems Nederland B.V. Due...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fosfomycin Tromethamine Granules for Oral Solution Recalled by Ascend...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dofetilide Capsules 500 mcg (0.5mg) Recalled by SUN PHARMACEUTICAL...
The Issue: Out of Specification result observed in content uniformity testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proclaim" XR 7 Implantable Pulse Generator (previously known Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.