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. 1,094 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,094 in last 12 months

Showing 16361–16380 of 30,087 recalls

Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Clarity Diagnostics Llc

Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...

The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...

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

Class III — Low RiskOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...

The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q. angiography system. Model 10848280 Recalled by Siemens Medical...

The Issue: Potential hardware issue which may cause thermal effects and possible damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...

The Issue: After a three year term, there is a potential for the external packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing