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. 2,451 recalls have been distributed to Arkansas in the last 12 months.
Showing 26781–26800 of 28,355 recalls
Recalled Item: The product is labeled in part "***Surgical Laser Technologies Recalled by...
The Issue: Firm became aware that some products within the specified lot may not have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is Recalled...
The Issue: Animas has identified a component issue affecting a small supply of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for...
The Issue: Lumenis Ltd is recalling certain models of VersaCut Morcellator devices to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Hybrids Recalled by Diagnostic Hybrids Inc Due to RhMK product...
The Issue: RhMK product fungal contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is including additional information and instructions in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage:...
The Issue: Veridex, LLC has received a report that a patient's demographics were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage:...
The Issue: Veridex, LLC has received a report that a patient's demographics were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: HeartWare, Inc. of Miami Lakes, FL is recalling their Ventricular Assist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade with...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Recalled by ConMed Corporation Due to ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...
The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade Recalled...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUR/Endoscopic Cable Recalled by ConMed Corporation Due to ConMed received...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED(R) ELECTROSURGICAL SAFETY HOLSTER Recalled by ConMed Corporation Due...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.