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. 1,932 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,932 in last 12 months

Showing 2440124420 of 30,087 recalls

Medical DeviceDecember 4, 2014· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...

The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: Rotoprone Therapy System. The Rotoprone Therapy System is an advanced...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Leonhard Lang Gmbh

Recalled Item: GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing...

The Issue: The firm discovered that during the use of these defibrillation electrodes a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Ferno-Washington Inc

Recalled Item: Ferno Model 35X PROFlexx Stretchers Recalled by Ferno-Washington Inc Due to...

The Issue: The wheel castor assemblies may be loosening on the stretchers.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)IR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Iris Diagnostics

Recalled Item: RTH8 Rotor Recalled by Iris Diagnostics Due to Iris International is...

The Issue: Iris International is recalling the RTH8 Rotor used in the StatSpin Express...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Teleflex Medical

Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...

The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Medtronic Sofamor Danek USA Inc

Recalled Item: POWEREASE Instruments Set Screw Breakoff Instrument Recalled by Medtronic...

The Issue: The retaining tabs component of the Set Screw Retaining Drive may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...

The Issue: Suboptimal routing of the cable may result in increased wear over time....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing