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. 2,716 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,716 in last 12 months

Showing 30213040 of 51,202 recalls

Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2025· Denison Pharmaceuticals, LLC

Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...

The Issue: Chemical Contamination: Presence of benzene.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
FoodFebruary 21, 2025· DANONE WAVE

Recalled Item: HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) Recalled by...

The Issue: The firm received complaints of spoilage and illness with the use of the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 21, 2025· DANONE WAVE

Recalled Item: CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL...

The Issue: The firm received complaints of spoilage and illness with the use of the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2025· One Source Nutrition, Inc,

Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 20, 2025· Central Admixture Pharmacy Services, Inc.

Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2025· BD SWITZERLAND SARL

Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...

The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2025· Orthofix U.S. LLC

Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...

The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2025· Microbiologics Inc

Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...

The Issue: The RSV target may give a late Ct value and could potentially not pass QC.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2025· Microbiologics Inc

Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...

The Issue: The A549 human cell target (human cells for sample adequacy control) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...

The Issue: There is a potential for the sterility of the device to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...

The Issue: There is a potential for the sterility of the device to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· Calyxo, Inc.

Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...

The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2025· MIM Software Inc

Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...

The Issue: In situations where two images with differing Fields of View (FOV) complete...

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

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2025· Turbare Manufacturing

Recalled Item: Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe Recalled by Turbare Manufacturing...

The Issue: Lack of Assurance of Sterility: due to a quality control process deviation....

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund