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. 2,558 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,558 in last 12 months

Showing 1626116280 of 28,172 recalls

Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T5 Zipper Toga with Peel-Away Face Shield Recalled by Stryker Instruments...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F Tesio CATHETER SET (CUFF 32CM FROM TIP) Recalled by Medical Components,...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F X 40CM TESIO CATHETER SET WITH "Y" ADAPTOR Recalled by Medical...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F X 60CM TESIO CATHETER SET WITH "Y" ADAPTOR Recalled by Medical...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F Tesio CATHETER SET (CUFF 22CM FROM TIP) Recalled by Medical Components,...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to There is...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: CATHETER REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: TWO PART ADAPTER Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: CATHETER REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to There is...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F MODIFIED Tesio CATHETER SET Recalled by Medical Components, Inc dba...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Zipper Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...

The Issue: Separation of material layers may occur, causing a potential risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing