Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,646 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,646 in last 12 months

Showing 1236112380 of 29,201 recalls

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· Insulet Corporation

Recalled Item: Omnipod DASH Personal Diabetes Manager (PDM) Recalled by Insulet Corporation...

The Issue: In certain scenarios, the Omnipod DASH PDM may suggest an inaccurate bolus...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2020· Merit Medical Systems, Inc.

Recalled Item: DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly Recalled by Merit...

The Issue: Vertebral hydraulic assemblies has incorrect expiration date printed on the...

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 Total Bilirubin_2 assay-In vitro Diagnostic for the...

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· 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· 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 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· 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· 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· 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: 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 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· 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· Carolina Liquid Chemistries Corp

Recalled Item: SPICE (JWH-018) CC443 Recalled by Carolina Liquid Chemistries Corp Due to...

The Issue: Corrections are being made to the device labeling regarding its intended...

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· 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