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. 2,558 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,558 in last 12 months

Showing 1624116260 of 28,172 recalls

Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Neonatal PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Kit Recalled by Vygon U.S.A. Due to Potential friction holes may affect...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Biomet, Inc.

Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...

The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes may...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Insertion Tray Recalled by Vygon U.S.A. Due to Potential...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD has...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Integrity Implants Inc.

Recalled Item: FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System)...

The Issue: Recently Integrity Implants uncovered a discrepancy in the cleaning...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Adult/Pediatric Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Radiometer Medical ApS

Recalled Item: AQURE Recalled by Radiometer Medical ApS Due to There is a potential problem...

The Issue: There is a potential problem relating to the AQURE System, versions 2.3.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Helena Laboratories, Corp.

Recalled Item: SPIFE Alkaline Hemoglobin Kit Recalled by Helena Laboratories, Corp. Due to...

The Issue: Lots of gel kits contained a newer revision of the Customer Procedures...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2018· Genesee BioMedical, Inc.

Recalled Item: Sternal Valve Retractors With Atrial and Aortic Rakes Recalled by Genesee...

The Issue: Failure in a retractor blade due to corrosion. In the area of the blade...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2018· Beaver-Visitec International Inc.

Recalled Item: Wet-Field Hemostatic Eraser Bipolar 25G Recalled by Beaver-Visitec...

The Issue: Products were packaged with incorrect labeling,

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

Class II — Potential Health HazardOngoing