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. 2,484 recalls have been distributed to Ohio in the last 12 months.
Showing 55021–55040 of 55,415 recalls
Recalled Item: SpineFrontier S-Lift Lock Shaft Inserter Recalled by SpineFrontier, Inc. Due...
The Issue: It has been verified through field use that there are two possible breakages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity¿ sampling device Recalled by US Endoscopy Group Inc Due to US...
The Issue: US Endoscopy received five complaints which noted difficulty in deploying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100 IQ Recalled by GE Healthcare, LLC Due to While...
The Issue: While performing a fluoroscopic examination on the GE Innova systems, there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3100-IQ Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3131-IQ Mobile X-ray system. The innova systems...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3100 Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actra-SX 500 Capsules Recalled by Body Basics Inc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA; product contains sildenafil, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telluride Percutaneous Rod Inserter Long Recalled by Biomet Spine, LLC Due...
The Issue: The Telluride Percutaneous Rod Inserter Long does not contain a feature that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Eon Mini Neurostimulation (IPG) System (Model 3788) is a 16-channel...
The Issue: As of 11/30/2011, St. Jude Medical has received 110 patient complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon (Model 3716) IPG is a dual channel Recalled by Advanced Neuromodulation...
The Issue: As of 11/30/2011, St. Jude Medical has received 110 patient complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini Neurostimulation (IPG) System (Model 3788) Recalled by Advanced...
The Issue: The firm has received 112 complaints of the Eon Mini IPGs that lost the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron Systems Synchron Calibrator Multi Calibrator Diskettes Recalled by...
The Issue: The recall was initiated because Beckman Coulter has confirmed a mislabeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Instrument System Recalled by Beckman Coulter...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the DxH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Stainer Floor Cabinet Recalled by Beckman...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the DxH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vector TAS Modular Driver Recalled by Ormco/Sybronendo Due to The...
The Issue: The Instructions For Use (IFUs) for Vector TAS Modular Driver for some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm)...
The Issue: Some of the sterile packages had broken seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Slide Processor. The PrepStain System is a liquid-based thin...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a Recalled by Tripath...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Upgrade Kit: 1.3.0.3/1.2 DiTi Cone. The PrepStain System is...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain PM Kit Recalled by Tripath Imaging, Inc. Due to Some Prep Stain...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.