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. 2,672 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,672 in last 12 months

Showing 1054110560 of 13,548 recalls

DrugApril 16, 2015· Tarmac Products, Inc.

Recalled Item: Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle...

The Issue: Products failed the Antimicrobial Effectiveness Test

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 16, 2015· Tarmac Products, Inc.

Recalled Item: Well at Walgreens Regular Strength Comfort Gel Cherry Flavor Recalled by...

The Issue: Products failed the Antimicrobial Effectiveness Test

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max DM Max Recalled by Reckitt Benckiser LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Night Time Cold & Flu Recalled by Reckitt Benckiser LLC Due...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Cold Recalled by Reckitt Benckiser LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast-Max Cold & Sinus Recalled by Reckitt Benckiser LLC Due to...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Severe Congestion & Cough Recalled by Reckitt Benckiser LLC...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Sandoz, Inc

Recalled Item: Cetirizine HCl Chewable Tablet Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Recalled by Reckitt...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2015· Actavis Laboratories

Recalled Item: Flurandrenolide Tape Recalled by Actavis Laboratories Due to Subpotent Drug:...

The Issue: Subpotent Drug: Flurandrenolide is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP Recalled by...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: HEPARIN Sodium Injection USP Recalled by Pharmedium Services, LLC Due to...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: HEPARIN Sodium Injection USP 25 Recalled by Pharmedium Services, LLC Due to...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Product recalled due to an elevated level of a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Product recalled due to an elevated level of a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Hospira Inc.

Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund