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. 1,955 recalls have been distributed to Ohio in the last 12 months.
Showing 21841–21860 of 30,087 recalls
Recalled Item: Richard-Allan Scientific Paraffin Type 3 For in vitro diagnostic use....
The Issue: Multiple complaints were received from customers indicating that they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verso Shoulder Forked Retractor (Comprehensive Instrumentation 2 Prong...
The Issue: Zimmer Biomet Inc. Verso Shoulder Forked Retractor (Comprehensive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC unit because a component on the PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SurePathTM Preservative Collection Vials Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of BD SurePath" collection vials associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instinct¿ Java¿ System (IFU : 046WAN0000T) . Stabilizes one or Recalled by...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm X 12o Solitaire Ti Medium Spacer Solitaire Anterior Spinal System...
The Issue: Zimmer Biomet Spine initiated a recall of certain Solitaire Ti Spacers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration with Tomosynthesis functionality Recalled by Siemens...
The Issue: A potential system fatal error may occur during tomosynthesis reconstruction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helioseal Clear 1 x 1.25 g Recalled by Ivoclar Vivadent, Inc. Due to...
The Issue: Complaints were received claiming the material failed to polymerize under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Inform II Base Unit as a part of the Recalled by Roche Diagnostics...
The Issue: Accu-Chek Inform II Base Unit might produce physical transmission errors in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.