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. 2,645 recalls have been distributed to Arkansas in the last 12 months.
Showing 3741–3760 of 28,355 recalls
Recalled Item: The Non-Sterile Flyte hood covers the user s head and Recalled by Stryker...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neurostimulation Kit (Ported Recalled by Nalu Medical, Inc. Due to...
The Issue: Neurostimulation Systems have a manufacturing non-conformance that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This product is a single use sterile device that is Recalled by Stryker...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Recalled by Stryker Corporation Due to Expired Products distributed...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Kittner Blunt Dissecting Instrument Recalled by ASPEN SURGICAL...
The Issue: The affected products may have been packaged with a defect in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nanoplasty 3D Bunion Correction System Implant Recalled by Treace Medical...
The Issue: Potential issue causing a higher frequency of interference with locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC-KEY* Gastric-Jejunal Feeding Tube Kit Recalled by Avanos Medical, Inc....
The Issue: The IFU was missing some risk information requested by another country to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium SuperPulsed Laser System Recalled by Olympus Corporation of...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser System Recalled by Olympus Corporation of the...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive SuperPulsed Laser System Wireless Footswitch Recalled by Olympus...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX Recalled by...
The Issue: Issue with analyzer when the pH of the calibration solution decreases during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Stryker Sustainability Solutions Due to Mislabeling
The Issue: Mislabeling; tourniquet cuff packaging labeled as dual port single bladder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for...
The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Powerheart G5 AED Recalled by Zoll Medical Corporation Due to G5...
The Issue: G5 Semi-Automatic AED is shipped, with a protective film over its front...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed...
The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Vertix MD - The Vertix MD Trauma has been Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MP - Intended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.