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. 1,908 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,908 in last 12 months

Showing 2746127480 of 30,087 recalls

Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHOS Slides packaged as 300 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products ALKP Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products SALI Slides packaged as 90 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PROT Slides packaged as 90 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Accelerated Care Plus Corporation

Recalled Item: Omnicycle Elite Recalled by Accelerated Care Plus Corporation Due to An...

The Issue: An anomaly in the firmware that may cause Omnicycle Elite to operate at a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Physio Control, Inc.

Recalled Item: The LIFEPAK 500 Automated External Defibrillator is a semi-automatic...

The Issue: The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes CMF Distraction System The product is intended for use Recalled by...

The Issue: The firm initiated a voluntary recall of the BC Distractor Body which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Flexible Medullary Reamer. Intended to be used to facilitate...

The Issue: Due to the coiled design for this product, the product is difficult to clean...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Philips Healthcare Inc.

Recalled Item: Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography...

The Issue: The Instructions for Use (IFU) for the MobileDiagnost wDR fails to comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Inegra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Zimmer, Inc.

Recalled Item: Bigliani/Flatow¿ The Complete Shoulder Solution Recalled by Zimmer, Inc. Due...

The Issue: The firm is initiating a removal of one lot of the Bigliani/Flatow Humeral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· GE Healthcare It

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: GE has recently become aware of potential issues due to out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Recalled by Church & Dwight Inc Due to Church and Dwight...

The Issue: Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing