Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,598 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,598 in last 12 months

Showing 1322113240 of 28,172 recalls

Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: WS80A Diagnostic Ultrasound System Version 1.00.16 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: HS70A Diagnostic Ultrasound System Version 2.01.00 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
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