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. 1,967 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,967 in last 12 months

Showing 1840118420 of 30,087 recalls

Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom LOWER EXTREMITY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom PACEMAKER PACK (CARDIOLOGY) convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom GYN LAPAROSCOPY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom PACEMAKER TRAY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom CATH PACK convenience kits Recalled by Avid Medical, Inc. Due...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom DAVINCI PACK convenience kits Recalled by Avid Medical, Inc....

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom PV MINOR PACK convenience kits Recalled by Avid Medical, Inc....

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom ORTHO TRAY convenience kits Recalled by Avid Medical, Inc....

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom PACEMAKER PACK convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom SHOULDER ARTHROSCOPY convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom PLASTIC BASIN PACK convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom UPPER EXTREMITY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Pressure Disposable Pressure Display Sets Extends the pressure line...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom EXTREMITY PACK convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom ELECTRO PHYSIOLOGY PK convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom NEURO PK convenience kits Recalled by Avid Medical, Inc. Due...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing