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 13801–13820 of 30,087 recalls
Recalled Item: Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number...
The Issue: The sets are configured with quick connectors that have been assembled in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to Potential...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis system (pre-2003) Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis 8.3 Commander Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis Commander Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis 6.1 Commander Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer UDI:05700693930909 Recalled by Radiometer America Inc...
The Issue: Software Security; The action is being initiated because of software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...
The Issue: code 7-102 Liquid Sensor Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransWarmer Warming Infant Transport Mattress Recalled by CooperSurgical,...
The Issue: The firm updated the IFU in April 2019 to clarify that use of the...
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: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.