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. 2,460 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,460 in last 12 months

Showing 2636126380 of 49,744 recalls

Medical DeviceFebruary 26, 2018· Beaver-Visitec International Inc.

Recalled Item: Wet-Field Hemostatic Eraser Bipolar 25G Recalled by Beaver-Visitec...

The Issue: Products were packaged with incorrect labeling,

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2018· Paddock Laboratories, LLC.

Recalled Item: Evamist (estradiol transdermal spray) Recalled by Paddock Laboratories, LLC....

The Issue: Defective Delivery System: Potential that cracks in the vial neck near the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2018· Mckesson Packaging Services

Recalled Item: RANITIDINE Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Stability Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2018· AstraZeneca Pharmaceuticals LP

Recalled Item: Lynparza (olaparib) capsules 50 mg Recalled by AstraZeneca Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications; elevated levels of quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
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 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· GE Healthcare

Recalled Item: GE Healthcare Centricity PACS-IW Recalled by GE Healthcare Due to A database...

The Issue: A database handling error could occur during the image acquisition process...

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: 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· 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: 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· 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· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4 Zipper Toga (S/M) Recalled by Stryker Instruments Div. of Stryker...

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: 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 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: 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: 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· 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