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. 2,619 recalls have been distributed to Arkansas in the last 12 months.
Showing 10101–10120 of 28,355 recalls
Recalled Item: Femoral Angiography Drape Bulk Non-Sterile Recalled by Cardinal Health 200,...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Angiography Drape Sterile Recalled by Cardinal Health 200, LLC Due...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-View Clear Leggings Bulk Non-Sterile Recalled by Cardinal Health 200, LLC...
The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Recalled by Arthrex, Inc. Due to The color indicator on the...
The Issue: The color indicator on the proximal end of the shaft of the AR-8770-02 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems are advanced continuous-rotation computed tomography...
The Issue: Philips has internally detected an issue with the actuators used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Midline Catheter Dressing Change Kit with Statlock - Product Usage: Recalled...
The Issue: Evidence of face masks or other material in the seal in several kits,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to For some LINAC...
The Issue: For some LINAC types, merging clinical beams with beams of approximate dose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter...
The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI Recalled by...
The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...
The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Recalled by...
The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee Recalled by...
The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIROS D-Vial Prep Set Recalled by Sirtex Medical Limited Due to There is a...
The Issue: There is a potential presence of particulate matter in the D-Vial.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...
The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...
The Issue: The product may be contaminated with Burkholderia cepacia
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...
The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...
The Issue: Teleflex is voluntarily recalling the products above due to customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.