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 2538125400 of 28,172 recalls

Medical DeviceAugust 1, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...

The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Zimmer, Inc.

Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...

The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Nidek Inc

Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...

The Issue: Under certain circumstances, the Left eye image may be saved as the Right...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Edwards Lifesciences, LLC

Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...

The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Large Buttress Compression Nut For Blade Guide Sleeve TFN The Recalled by...

The Issue: The Large Buttress Compression Nut For Blade Guide Sleeve TFN was recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...

The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Fujinon Inc

Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...

The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Leica Biosystems Newcastle Ltd.

Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...

The Issue: The affected lots of the product may contain a contaminant of fungus that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...

The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...

The Issue: Synthes became aware that during a procedure using the Matrix Threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...

The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and...

The Issue: Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric...

The Issue: Certain lots of Trochanteric Fixation Nail were distributed to the field...

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

Class II — Potential Health HazardOngoing