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. 1,943 recalls have been distributed to Ohio in the last 12 months.
Showing 23821–23840 of 30,087 recalls
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Gloves Recalled by Covidien LLC Due to Devon Light...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Cobalt-Chrome Femoral Components Recalled by Biomet, Inc. Due to...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon Oval MRI System Recalled by Hitachi Medical Systems America...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System Recalled by Hitachi Medical Systems America Inc Due...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon MRI System Recalled by Hitachi Medical Systems America Inc...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remote Network Station Recalled by Nihon Kohden America Inc Due to Nihon...
The Issue: Nihon Kohden America (NKA) is recalling the Remote Network Station (RNS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the cable cart and the corrugated hose are unable to move freely, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - 8MM x 12.5MM Fluted Barrel Recalled by The Anspach Effort, Inc....
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...
The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - Fluted Drum Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH - 5MM Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...
The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.