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. 2,502 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,502 in last 12 months

Showing 2034120360 of 28,172 recalls

Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Aluminum crutch under the following labels: 1) Aluminum crutch Recalled by...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Acorn Stairlifts Inc

Recalled Item: Acorn 180 Curved Stairlift Recalled by Acorn Stairlifts Inc Due to Aluminum...

The Issue: Aluminum rivets holding the base squab to the framer under prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal aluminum crutch Recalled by Medical Depot Inc. Due to Tip crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Direct Supply aluminum crutch Recalled by Medical Depot Inc. Due to Tip...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: EZ adjust aluminum crutch under the following labels: 1) EZ Recalled by...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Biomet, Inc.

Recalled Item: Verso Shoulder Forked Retractor (Comprehensive Instrumentation 2 Prong...

The Issue: Zimmer Biomet Inc. Verso Shoulder Forked Retractor (Comprehensive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...

The Issue: Siemens found a defective part in their production line which could increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing