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 1450114520 of 28,172 recalls

Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Anti-HAV IgM test System Recalled by Roche Diagnostics Corporation Due to...

The Issue: Potential for erroneous result messages for the Anti-HAV IgM assay when run...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Meridian Bioscience Inc

Recalled Item: PREMIER Cryptococcal Antigen Recalled by Meridian Bioscience Inc Due to An...

The Issue: An enzyme reagent included in the kit is not maintaining stability through...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2018· Roche Diagnostics Corporation

Recalled Item: COBAS INTEGRA 400 plus analyzer used in the following assays: Recalled by...

The Issue: COBAS INTEGRA¿ 400 plus and cobas c 111 analyzers Additional Extra Wash...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2018· Roche Diagnostics Corporation

Recalled Item: cobas c 111 with ISE analyzers analyzer used in the Recalled by Roche...

The Issue: COBAS INTEGRA¿ 400 plus and cobas c 111 analyzers Additional Extra Wash...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2018· Bayer Medical Care, Inc.

Recalled Item: MAVIG Portegra or Portegra2 Overhead Counterpoise System (OCS) used in...

The Issue: If the head mount knob is not properly tightened and the operator directly...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2018· Arrow International Inc

Recalled Item: Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-44052-VPS2...

The Issue: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2018· Arrow International Inc

Recalled Item: Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-45052-VPS2...

The Issue: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2018· Elekta, Inc.

Recalled Item: MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology...

The Issue: There is a potential that Wedge IDs were not included in the DICOM RT PLAN...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Applied Medical Resources Corp

Recalled Item: GelPOINT Path Transanal Procedural Pack with Epix Electrosurgical L-Hook...

The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Applied Medical Resources Corp

Recalled Item: Epix Electrosurgical Probes with Smoke Evacuation Recalled by Applied...

The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Product Usage: The Proton Therapy System - Proteus Recalled by...

The Issue: There is a risk of detachment of the Compact Gantry Rolling Floor.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: AMIA Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic...

The Issue: Negative bias results when using VITROS VALP Reagent, GEN 25.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing