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. 2,535 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,535 in last 12 months

Showing 1980119820 of 28,172 recalls

Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software error in previous software versions in which two for the same image...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...

The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Immuno-Mycologics, Inc

Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...

The Issue: The device was found to have bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· Leica Biosystems Richmond Inc.

Recalled Item: Ariol is an automated scanning microscope and image analysis system....

The Issue: An issue during the manufacturing process caused systems to have an...

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

Class III — Low RiskOngoing
Medical DeviceMay 6, 2016· BEST THERATRONICS LTD.

Recalled Item: Best Theratronics cabinet x-ray systems intended for use in the Recalled by...

The Issue: It was discovered that both the new device and the predicate device failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· Custom Ultrasonics, Inc.

Recalled Item: The System 83 Plus Recalled by Custom Ultrasonics, Inc. Due to To warn...

The Issue: To warn customers that Custom Ultrasonics, Inc. System 83 Plus AERs should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Recalled...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker PowerPRO (XT Recalled by Stryker Medical Division of Stryker...

The Issue: Complaints of smoke coming from the foot end of the cot. This reportedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: VersaFx Femoral Fixation System Hex head compression screw 4.7 mm Recalled...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Periarticular plating system Recalled by Zimmer Manufacturing B.V. Due to A...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing