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. 2,614 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,614 in last 12 months

Showing 1210112120 of 28,172 recalls

Medical DeviceFebruary 24, 2020· Butterfly Network, Inc.

Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...

The Issue: Distributed without an approved 510(k)

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2020· LivaNova USA Inc.

Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...

The Issue: The firm is providing validated cleaning and disinfection instructions in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Qiagen Sciences LLC

Recalled Item: AmniSure ROM Test Recalled by Qiagen Sciences LLC Due to An image on the...

The Issue: An image on the associated polybag contains an incorrect rinse time of 30...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Radiometer Medical ApS

Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...

The Issue: Reports have been received about the transcutaneous monitoring system...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Philips North America, LLC

Recalled Item: Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software...

The Issue: Menu selections for users to access the oxygen (O2) sensor calibration were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2020· Haemonetics Corporation

Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...

The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Tests returning incorrect...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· James Leckey Design Ltd

Recalled Item: Firefly Floorsitter Recalled by James Leckey Design Ltd Due to The firm...

The Issue: The firm received reports of a number of broken latches on the floorsitter.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Randox Laboratories Ltd.

Recalled Item: Chemistry QC Premium Plus Recalled by Randox Laboratories Ltd. Due to The...

The Issue: The control target and range value for Sodium using the ISE indirect method...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing