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. 2,506 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,506 in last 12 months

Showing 2686126880 of 51,202 recalls

DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN PLUS Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-PLEX Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: ADENO-PLEX Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN EXTREME Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: METHYLCOBALAMIN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park...

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 5, 2018· Visaris DOO

Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...

The Issue: A failure of the tube arm suspension is possible while the tube arm height...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2018· Visaris DOO

Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...

The Issue: A failure of the tube arm suspension is possible while the tube arm height...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2018· Abbott

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...

The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 5, 2018· Visaris DOO

Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...

The Issue: A failure of the tube arm suspension is possible while the tube arm height...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Handpiece Headquarters

Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...

The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...

The Issue: The DC power to the IFOSS collision detector control panel at your facility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Menarini Silicon Biosystems

Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...

The Issue: Unusually high number of total images/unassigned events may require...

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

Class II — Potential Health HazardOngoing
DrugApril 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Bendeka 25 mg/mL 4 mL MDVPF NDC 63459-0348-04 28 days supply Recalled by...

The Issue: Lack of Processing Controls.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Otezla 30 mg tablet NDC 59572-0631-06 30 days supply Recalled by Kroger...

The Issue: Lack of Processing Controls.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Altera Handset NDC 83490-0678-05 56 days supply Recalled by Kroger Specialty...

The Issue: Lack of Processing Controls.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Capecitabine 500 mg Tablet NDC 00378-2512-78 28 days supply and 21 days...

The Issue: Lack of Processing Controls.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund