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. 2,806 recalls have been distributed to Ohio in the last 12 months.
Showing 2561–2580 of 30,087 recalls
Recalled Item: Access Intact PTH assay Recalled by Beckman Coulter, Inc. Due to Beckman...
The Issue: Beckman Coulter has identified that some Access PTH reagent packs from lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Mini Enteral Extension Set Recalled by Applied Medical Technology Inc...
The Issue: The extension sets subject to this recall have ENFit connections, although...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...
The Issue: Due to an increase of complaints for bracket bond failures and skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...
The Issue: Potential for procedural delays or interruptions during use of the Auryon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver with Software Recalled by Spacelabs Healthcare,...
The Issue: Telemetry receivers with affected software versions may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse PRO The Spacelabs model 98700 is a Recalled by Spacelabs Healthcare,...
The Issue: Due to a manufacturing error the incorrect device serial number was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Mini The Eclipse MINI Model 98900 is Recalled by Spacelabs...
The Issue: Due to a manufacturing error the incorrect device serial number was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code Recalled...
The Issue: Due to complaints received for the marker band detaching from the distal tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.