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. 2,591 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,591 in last 12 months

Showing 1428114300 of 28,172 recalls

Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Optima PET/CT 560 Recalled by GE Healthcare, LLC Due to GE Healthcare PET/CT...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...

The Issue: Packaged with an incorrect size inner cannula.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...

The Issue: Incorrect needle length and gage.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Fenwal Inc

Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...

The Issue: The optional Vacuum Unit may stop working and display the failure message...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Canon Medical System, USA, INC.

Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...

The Issue: Table tilts without operator involvement as a result of liquid spilling into...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...

The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 8, 2019· Draegar Medical Systems, Inc.

Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...

The Issue: The firm is recalling their Delta family of patient monitors software due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Draegar Medical Systems, Inc.

Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...

The Issue: The firm is recalling their Delta family of patient monitors software due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...

The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...

The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.

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

Class II — Potential Health HazardOngoing