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. 1,967 recalls have been distributed to Ohio in the last 12 months.
Showing 17861–17880 of 30,087 recalls
Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...
The Issue: While reviewing documentation for the next software release of the 2008T, an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESONATE EL ICD DR Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOMENTUM X4 CRT-D Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIGILANT X4 CRT-D Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESONATE X4 CRT-D Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESONATE EL ICD VR Recalled by Boston Scientific Corporation Due to The...
The Issue: The devices have an incorrect firmware configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Shaft hip and anatomical shoulder instrument used for preparation...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling
The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirus Drill 13mm diameter trauma instrument used for preparation of Recalled...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...
The Issue: Pre-procedural issues related to software defects
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...
The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) Recalled...
The Issue: Correction to update sterilizer software to prohibit the use of expired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous...
The Issue: A specific lot of the FlexFlowTM Venous Cannula, 200-200, is being recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.