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. 2,590 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,590 in last 12 months

Showing 1496114980 of 28,172 recalls

Medical DeviceAugust 28, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...

The Issue: There is a potential to generate falsely elevated serum or plasma chloride...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...

The Issue: The reagent pack exhibits the potential for an increased frequency of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Stryker GmbH

Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...

The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass System 241-S Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass ULTRA SYSTEM Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Alcon Research, LTD.

Recalled Item: CyPass System 241 Recalled by Alcon Research, LTD. Due to Analysis of the...

The Issue: Analysis of the completed dataset from the COMPASS-XT long-term study showed...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due...

The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due...

The Issue: Screws on a Terumo¿ Advanced Perfusion System 1 Power Manager Board (the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2018· Arthrex, Inc.

Recalled Item: Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product...

The Issue: The Li-ion Battery Housing for the AR-400 DrillSaw Sports 400 System may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Lipase Recalled by Beckman Coulter Inc. Due to NAPQI, a...

The Issue: NAPQI, a metabolite of Acetaminophen, causes negative interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Uric Acid Recalled by Beckman Coulter Inc. Due to NAPQI, a...

The Issue: NAPQI, a metabolite of Acetominophen, causes negative interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco MEM Non-Essential Amino Acids Solution (100X) (SKU 11140050) Recalled...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco GlutaMAX Supplement Recalled by Life Technologies, Corp. Due to Leaky...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco DPBS Recalled by Life Technologies, Corp. Due to Leaky bottles due to...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco Sodium Pyruvate (100 mM) SKU 11360070 Recalled by Life Technologies,...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Vision RT Ltd

Recalled Item: Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant...

The Issue: RTInterface error in the event of an I/O error between the IGC PCB and the...

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

Class II — Potential Health HazardOngoing