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. 2,365 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,365 in last 12 months

Showing 4504145060 of 49,744 recalls

Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Acuson SC2000 volume imaging ultrasound systems at software version 3.0....

The Issue: Software issue results in inaccurate 3D image may result in ablation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Medical Indicators, Inc.

Recalled Item: Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A....

The Issue: TempaDot products may have been mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Pemco Inc

Recalled Item: Rultract Retractor Ratchet Cover Plate Distributed by Pemco Recalled by...

The Issue: The firm became aware of the problem when a ratchet cover plate on a device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2013· Medtronic Xomed, Inc.

Recalled Item: Tray Surgical Recalled by Medtronic Xomed, Inc. Due to The firm will recall...

The Issue: The firm will recall and replace the identified instrument trays in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Baxter Healthcare Corp.

Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to the white printed paper...

The Issue: the white printed paper layer on the pouch packaging may not be fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Becton Dickinson & Co.

Recalled Item: PrepStain AG. For use in the screening and detection of cervical cancer....

The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Becton Dickinson & Co.

Recalled Item: PrepStain Tecan US-II. For use in the screening and detection Recalled by...

The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Becton Dickinson & Co.

Recalled Item: PrepStain Tecan US-I. For use in the screening and detection Recalled by...

The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker 1) Asnis III Cannulated Screw 4.0x40mm TL Recalled by Stryker...

The Issue: Stryker received a report that the length of the cannulated screw asnis III,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Sorin Group USA, Inc.

Recalled Item: Edwards Lifesciences Suction Wand Model S099B Recalled by Sorin Group USA,...

The Issue: Sorin Group is recalling certain lots of Edwards Lifesciences Suction Wand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Mullins Transseptal Adult 7F Recalled by Medtronic Inc. Cardiac...

The Issue: Medtronic identified a specific labeling issue for specific lots of Mullins...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Philips Healthcare Inc.

Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...

The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2013· Radiometer America Inc

Recalled Item: pCO2 D788 Membranes. Distributed by Radiometer America Recalled by...

The Issue: RADIOMETER has become aware that some D788 pCO2 membranes can cause biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The patient support may move in an unintended manner if the footswitch cover...

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

Class II — Potential Health HazardOngoing
DrugJuly 4, 2013· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurites/Degradation Specifications: Test failure of single largest...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 4, 2013· Whole Foods Market

Recalled Item: Crave Brothers Les Freres cheese sold with labeling as: Les Freres Recalled...

The Issue: Whole Foods Market announces that it is recalling Crave Brothers Les Freres...

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

Class I — Serious Health HazardOngoing
Refund