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 1926119280 of 28,172 recalls

Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 400 Measurement Cartridge Siemens SMN numbers:10329756...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 405 Measurement Cartridge Siemens SMN numbers: 10844812...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2016· Arrow International Inc

Recalled Item: HANDS-OFF Infusion Port Thermodilution Catheter consists of the Arrow IPTD...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Heritage Medical Products, Inc.

Recalled Item: 2000 Vascular with 30 Degree option Recalled by Heritage Medical Products,...

The Issue: Potential for bed to drop suddenly at the head while a patient is laying on it.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to RaySearch became...

The Issue: RaySearch became aware of the problem as it was discovered in cooperation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2016· Ormco/Sybronendo

Recalled Item: Sealapex Xpress Recalled by Ormco/Sybronendo Due to SybronEndo is recalling...

The Issue: SybronEndo is recalling the Sealapex Xpress because it was labeled with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2016· GE Healthcare, LLC

Recalled Item: GE Healthcare SIGNA Creator Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare is conducting a recall dealing with an incorrect RF Power...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Carry bar which is an accessory to a lift used Recalled by ErgoSafe...

The Issue: The black plastic puck on the carry bar is breaking resulting in potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· ConMed Corporation

Recalled Item: CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter Recalled by ConMed...

The Issue: CONMED received complaints of damage to the CS-023 electrodes shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic V40 Femoral Head Recalled by Stryker Howmedica Osteonics Corp....

The Issue: Stryker received several complaints describing incidence of harm secondary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Trimed Inc

Recalled Item: TriMed Semi-Tubular Plate Recalled by Trimed Inc Due to TriMed is recalling...

The Issue: TriMed is recalling the Semi-Tubular Plates with 10 holes (SMTP-10) because...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - Recalled by...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Smith & Nephew, Inc.

Recalled Item: TANDEM (TM) INTL COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew,...

The Issue: Some Bipolar shells were manufactured with an out of specification retainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Smith & Nephew, Inc.

Recalled Item: TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew, Inc....

The Issue: Some Bipolar shells were manufactured with an out of specification retainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Maximal Barrier Recalled...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Recalled...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: SENSAR 1-Piece IOL Recalled by Abbott Medical Optics Inc. (AMO) Due to...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS Multifocal Foldable Acrylic Intraocular Lens Recalled by Abbott...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing