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 8261–8280 of 28,355 recalls
Recalled Item: Separation Technology Creamatocrit Plus Recalled by Stanbio Laboratory, LP...
The Issue: The device was being marketed as an IVD without a 510(k). Therefore,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology Recalled...
The Issue: Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cub 2 Enclosed Bed Canopy System Recalled by Sensory Medical Inc Due to Due...
The Issue: Due potential misuse of the product, firm is updating warnings and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Resources International First Aid Kits Recalled by Total Resources...
The Issue: ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Resources International First Aid Kits Recalled by Total Resources...
The Issue: ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VELYS Robotic-Assisted Solution Base Product No.: 451570100 Recalled by...
The Issue: System software v1.5.1 has a system software issue related to the Daylight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virus Counter Platform with Model Name VC3100 Recalled by Sartorius...
The Issue: The Virus Counter is an automated laboratory instrument that enables rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus 30 Priority Pack w/.096 RHV - WPL2122277-01 Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDEFLATOR Plus 30 - WPL2122277-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 INDEFLATOR - WPL2122268-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack Accessory Kit/.096 RHV - WPL2122270-01 Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.