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. 2,666 recalls have been distributed to Arkansas in the last 12 months.
Showing 301–320 of 28,355 recalls
Recalled Item: TS-10/TS-10H Tube Sorter Recalled by Sysmex America, Inc. Due to Under...
The Issue: Under specific conditions, the lift's electromagnetic holding force may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Recalled by Intuitive Surgical, Inc. Due to Access Port System...
The Issue: Access Port System tray may develop cracks potentially resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10F Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is...
The Issue: Potential for defect for Asserachrom HPIA lot 271288, which can affect every...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum Duo Infusion System Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical received one lot of defective primary speakers from our supplier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Philips has identified that in a limited number of impacted systems the drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.