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. 2,614 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,614 in last 12 months

Showing 1214112160 of 28,172 recalls

Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Direct Bilirubin_2 assay-SMN: 10316610 (20 mL) & 10341114...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Total Bilirubin Flex¿ reagent cartridge -In vitro...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the Recalled by...

The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Microbiologics Inc

Recalled Item: Microbiologics QC SETS AND PANELS Recalled by Microbiologics Inc Due to...

The Issue: KWIKSTIK 2 Pack () and QC Set and Panels: KWIKSTIK YST Comprehensive QC Set...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK 2 Pack Trichosporon dermatis derived from ATCC 204094 (Catalog#...

The Issue: KWIKSTIK 2 Pack () and QC Set and Panels: KWIKSTIK YST Comprehensive QC Set...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific released a new Software Update Application that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2020· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific released a new Software Update Application that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2020· Boston Scientific Corporation

Recalled Item: Imager II 5F Angiographic Catheters Recalled by Boston Scientific...

The Issue: Potential for tip detachment of Imager II 5F Angiographic Catheters

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 11, 2020· Intellijoint Surgical, Inc.

Recalled Item: Intellijoint Navigation System Recalled by Intellijoint Surgical, Inc. Due...

The Issue: During total knee arthroplasty (TKA), the software may incorrectly calculate...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: McKesson Cardiology ECG Management Recalled by CHANGE HEALTHCARE CANADA...

The Issue: Inaccurate estimation of the heart rate may occur in instances where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Stick Sponge Presaturated W/PVP DYND70288H 2/PK Expiration Recalled...

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Sterile 3mL Syringes with 21GA x 1 Inch Needle Recalled by Medline...

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Winged Sponges Presaturated W/PVP DYND70289H Expiration 06/30/2022....

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Agfa N.V.

Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- Recalled...

The Issue: Tomosynthesis image acquisition sequence did not stop automatically after...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio Recalled by Siemens Medical Solutions USA, Inc Due to The Ysio system...

The Issue: The Ysio system may process incorrect internal values for the position of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 88-Series-washer disinfectors intended for cleaning Recalled by...

The Issue: Potential leakage that may occur due to ruptured spot welds in the chamber,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Covidien Llc

Recalled Item: Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed...

The Issue: Sterile packaging may potentially be compromised, and use of products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Covidien Llc

Recalled Item: Covidien Force TriVerse Electrosurgical Devices Recalled by Covidien Llc Due...

The Issue: Sterile packaging may potentially be compromised, and use of products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2020· Integra LifeSciences Corp.

Recalled Item: NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to...

The Issue: Nonconforming product which was dispositioned for rejection was mistakenly...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 7, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys CA 19-9 Recalled by Roche Diagnostics Operations, Inc. Due to The...

The Issue: The firm has received an increased number of complaints concerning...

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

Class II — Potential Health HazardOngoing