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. 2,598 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,598 in last 12 months

Showing 1298113000 of 28,172 recalls

Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· GE Healthcare, LLC

Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...

The Issue: Potential for failure of the patient leakage current test. There is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2019· Draegar Medical Systems, Inc.

Recalled Item: The Infinity Acute Care System (IACS) Monitoring Solution with the Recalled...

The Issue: Cybersecurity vulnerabilities may cause device to reboot, lose alarm...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Merit Medical Systems, Inc.

Recalled Item: Custom Sheath Introducer Kit - Product Usage: intended Recalled by Merit...

The Issue: labeling error: Due to a manufacturing issue, product package was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Olympus Corporation of the Americas

Recalled Item: Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System -...

The Issue: Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M1356A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Tocotransducer (Nautilus) 2264LAX Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco MP Transducer (M2734B) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V60 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco M2734A Recalled by Pacific Medical Group Inc. Due to Fetal/maternal...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-Touch Screen Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: External Toco Transducer (M1355A) Recalled by Pacific Medical Group Inc. Due...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing