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.
Showing 16361–16380 of 30,087 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: The flow rate test verification was not properly executed for certain Sigma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.