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. 2,628 recalls have been distributed to Arkansas in the last 12 months.
Showing 6641–6660 of 28,355 recalls
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880473001 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 800756005 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880405003 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: regard Item Number: 800718003 Recalled by...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaOne Reusable Positioning Cannula 12mm Standard Recalled by Covidien LP...
The Issue: There is a manufacturing non-conformance that may result in a metal shaving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaOne Reusable Positioning Cannula 8 mm Standard Recalled by Covidien LP...
The Issue: There is a manufacturing non-conformance that may result in a metal shaving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software Recalled by...
The Issue: Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion System with software versions: R2.2.O Recalled by PHILIPS...
The Issue: Potential Loss of X-ray-When the full disk capacity is reached, X-Ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and...
The Issue: Potential for the spring to become loose and fall out of the device, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS one with a hybrid cable- An angiography system developed Recalled by...
The Issue: Examination room monitor connected with the hybrid cable may have a display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813...
The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814...
The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DERMLITE DL4W Recalled by DermLite LLC Due to Incorrect labeling; Package...
The Issue: Incorrect labeling; Package labeling contains a different serial number then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...
The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery....
The Issue: Device suddenly and forcefully disassembled after cryotherapy, potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SenSight Extension Tunneler Kit Recalled by Medtronic...
The Issue: Medtronic has received reports of SenSight Extension Tunneler kits that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integre Pro Yellow LP561 Recalled by Ellex Medical Pty Ltd. Due to When...
The Issue: When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Cortisol 50T (Material Number 10995538) Recalled by Siemens...
The Issue: There is a negative bias with urine patient samples and urine cortisol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.