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. 2,580 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,580 in last 12 months

Showing 2754127560 of 55,415 recalls

FoodJune 22, 2018· Talking Rain Beverage Co Inc

Recalled Item: Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water Recalled by...

The Issue: Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm...

Recommended Action: Do not consume. Return to store for a refund or discard.

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

Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...

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· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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: 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: 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: 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: 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