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. 2,484 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,484 in last 12 months

Showing 5530155320 of 55,415 recalls

Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Knife Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2009· Alere San Diego, Inc.

Recalled Item: Triage TOX Drug Screen Panel Recalled by Alere San Diego, Inc. Due to...

The Issue: Biosite is recalling the Triage TOX Drug Screen kits where the box...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2009· Spinal Elements, Inc

Recalled Item: Mercury Spinal System DIA 5.5 x 50mm Straight Rod Recalled by Spinal...

The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2009· Spinal Elements, Inc

Recalled Item: Mercury Spinal System DIA 5.5 x 110mm Straight Rod Recalled by Spinal...

The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2009· Spinal Elements, Inc

Recalled Item: Mercury Spinal System DIA 5.5 x 40mm Straight Rod Recalled by Spinal...

The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2009· Spinal Elements, Inc

Recalled Item: Mercury Spinal System DIA 5.5 x 30mm Straight Rod Recalled by Spinal...

The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2009· Spinal Elements, Inc

Recalled Item: Mercury Spinal System DIA 5.5 x 70 MM Lordosed Rod Recalled by Spinal...

The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2009· Spinal Elements, Inc

Recalled Item: Mercury Spinal System DIA 5.5 x 30 MM Lordosed Rod Recalled by Spinal...

The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2009· Spinal Elements, Inc

Recalled Item: Mercury Spinal System DIA 5.5 x 60mm Straight Rod Recalled by Spinal...

The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...

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

Class III — Low RiskOngoing