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. 1,943 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,943 in last 12 months

Showing 2372123740 of 30,087 recalls

Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Major General Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Bayview Breast Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Knee Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Basic Kit Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Virginia Custom Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Hernia Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Head Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Custom Arterial Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: General Pack II Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Basic Tray Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2015· Spacelabs Healthcare Inc

Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...

The Issue: Modules resetting. This failure mode happens when the Spacelabs Command...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· ICU Medical, Inc.

Recalled Item: 98" (249 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...

The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Suction Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Glaucoma Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Knee Arthro Pack and Knee Arthro Pack II - contains Recalled by Stradis...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Lima Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Mississippi Pack - contains Devon Light Glove Used during surgery Recalled...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Arthroscopy Pack - contains Devon Light Glove Used during surgery Recalled...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Phleb Pack and Laser Phleb Pack - contains Devon Light Recalled by Stradis...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Shoulder Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing