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. 1,114 recalls have been distributed to Ohio in the last 12 months.
Showing 14501–14520 of 55,415 recalls
Recalled Item: DREAMTOME 44-30MM/450CM Material Number: M00584070 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-20-260-035 Material Number: M00573000 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-450-035 Material Number: M00573030 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 49-30MM/450CM Material Number: M00584030 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-260-035 Material Number: M00573020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 49-20MM/260CM Material Number: M00584000 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-30MM/260CM Material Number: M00583050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME REVOLUTION RX 39-20-260-025 Material Number: M00584240 Recalled by...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-20-450-025 Material Number: M00573090 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-30-260-025 Material Number: M00573100 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 44-30MM/260CM Material Number: M00584050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 49-20MM/260CM Material Number: M00583000 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 44-20-260-035 Material Number: M00573040 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-20MM/450CM Material Number: M00583060 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-30MM/450CM Material Number: M00583070 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM TRIVANTAGE EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due...
The Issue: There is potential for multiple issues due to a manufacturing nonconformity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SonarMed AirWave Monitor Kit (Monitor Recalled by Covidien, LP Due to Prior...
The Issue: Prior to use on a patient, the device alarm speaker failed to annunciate on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Repair Kit Recalled by Philips Respironics, Inc. Due to Philips...
The Issue: Philips has identified a specific lot of non-conforming material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Philips has...
The Issue: Philips has identified a specific lot of non-conforming material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors -...
The Issue: The External Retention Bolster contained in the kit may be a larger diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.