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 2186121880 of 52,570 recalls

FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Winco Foods Recalled by CH Guenther & Sons, Inc Due to Potential Salmonella...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Williams Original Chili Seasoning Recalled by CH Guenther & Sons, Inc Due to...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: HEB Taco Seasoning Mix 25% Less Sodium Net Wt. 1.25 OZ Recalled by CH...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Great Value Mild Taco Seasoning Recalled by CH Guenther & Sons, Inc Due to...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Williams Ingredients Recalled by CH Guenther & Sons, Inc Due to Potential...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 24, 2019· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc. Due to...

The Issue: Potential for Hemospray device to be unable to spray powder due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle Recalled by Allergan PLC Due to The action was initiated following...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle133 Plus Tissue Expander With/Without Suture Tabs Recalled by...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Komuro Recalled by Allergan PLC Due to The action was initiated following...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 150 Full Height and Short Height Implants Recalled by Allergan PLC...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle Inspira Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: McGhan Croissant-Shaped Tissue Expanders Recalled by Allergan PLC Due to The...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 410 Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 510 Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: McGhan BioDIMENSIONAL silicone-Filled Breast Implants Recalled by Allergan...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing