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 2718127200 of 30,087 recalls

Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2013· Villa Radiology Systems LLC

Recalled Item: Juno DRF System. Mobile X-ray system These are general Recalled by Villa...

The Issue: It has been discovered that the Air Kerma rate information is inconsistent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Nidek Inc

Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...

The Issue: Under certain circumstances, the Left eye image may be saved as the Right...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...

The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Zimmer, Inc.

Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...

The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...

The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...

The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...

The Issue: Synthes became aware that during a procedure using the Matrix Threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Fujinon Inc

Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...

The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Edwards Lifesciences, LLC

Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...

The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...

The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Leica Biosystems Newcastle Ltd.

Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...

The Issue: The affected lots of the product may contain a contaminant of fungus that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used Recalled by...

The Issue: Complaints were received of inconsistencies in the expiration dates shown on...

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

Class II — Potential Health HazardOngoing