Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,769 recalls have been distributed to Ohio in the last 12 months.
Showing 6781–6800 of 30,087 recalls
Recalled Item: STA Compact Max fully automatic clinical analyzer Recalled by Diagnostica...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA R Max fully automatic clinical instrument designed to perform Recalled...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: regard Item Number 800706005 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: Sterile surgical convenience kit: regard Item Number: 800753005 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: Sterile surgical convenience kit: regard Item Number: 880393003 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 11mm 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: Sterile surgical convenience kits: 1. regard Item Number: 880353009 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: 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.