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. 1,959 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,959 in last 12 months

Showing 1904119060 of 30,087 recalls

Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain Recalled by...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Teleflex Medical

Recalled Item: INFANT 20/BX Recalled by Teleflex Medical Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Flat Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Silicone Round Drain Recalled by Cardinal Health 200, LLC Due...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P638) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P605) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· EBI Patient Care, Inc.

Recalled Item: 10-1398M - SpF-PLUS Implantable Stimulator. Indicated as a spinal fusion...

The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-GN80) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· EBI Patient Care, Inc.

Recalled Item: 10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a Recalled...

The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N268) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N351) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N300) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P607) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N222) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing