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. 2,591 recalls have been distributed to Arkansas in the last 12 months.
Showing 11841–11860 of 28,355 recalls
Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-Hydroxybutyrate LiquiColor Recalled by Cardinal Health Inc. Due to Three...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strep B Carrot Broth One-Step Recalled by Cardinal Health Inc. Due to Three...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha VA30-mobile X-Ray system Recalled by Siemens Medical...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha VA20-mobile X-Ray system Material # 10308191 The Recalled...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Spin VA30-mobile X-Ray system Recalled by Siemens Medical...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrysof Recalled by Alcon Research LLC Due to Incorrect IOL diopter
The Issue: Incorrect IOL diopter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Low Weight-Low Volume Blood Transport System for...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Set Prime Line - Product Usage: is Recalled by Baxter...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Transport System for Hemodialysis Blood Set -...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Low Volume Blood Transport System for Hemodialysis Blood...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 154335 Oxford Partial Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 184762 Knees Vanguard Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: TMJPM-1510 Microfixation Custom Made Device Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 189260 Vanguard Knee System Recalled by Biomet, Inc. Due to...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 155308 Knees AGC Knee System PS Molded Tibial Component...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Spin Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: The unplugging of the main cable on the monitor trolley from the X10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremities Item Number: 1)113954 Hybrid Glenoid Glenoid Base Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.