Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,945 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,945 in last 12 months

Showing 1860118620 of 29,298 recalls

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· 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· Teleflex Medical

Recalled Item: PE CONNECTOR 3/8 STRAIGHT 20/BX Recalled by Teleflex Medical Due to...

The Issue: Labeling: The expiration date is not stated on the labeling, there is a...

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 Flat 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 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 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· 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 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· JAS Diagnostics Inc.

Recalled Item: Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent Recalled by...

The Issue: May result in elevated platelet backgrounds during routine...

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· Teleflex Medical

Recalled Item: PE CONNECTOR 5 IN 1 20/BX Recalled by Teleflex Medical Due to Labeling: The...

The Issue: Labeling: The expiration date is not stated on the labeling, there is a...

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 Bacillus identification card (BCL) Recalled by Biomerieux Inc Due to...

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 Fungal Susceptibility card (AST-YS05) 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-P600) 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-P631) 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