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. 2,674 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,674 in last 12 months

Showing 97819800 of 13,548 recalls

DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Health Best Choice Care Recalled by Ohm Laboratories, Inc. Due to...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Meijer Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Health Mart Pharmacy loratadine orally disintegrating tablets Recalled by...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Safeway Care Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Sunmark loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Leader Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: QC Quality Choice Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Wal-itin Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Fred's Loratadine Orally Disintegrating Tablets Recalled by Ohm...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Ohm Laboratories, Inc.

Recalled Item: CareOne Original Prescription Strength Recalled by Ohm Laboratories, Inc....

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
DrugJuly 28, 2015· Fresenius Kabi USA, LLC

Recalled Item: Hydralazine Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...

The Issue: Incorrect Expiration Date: The "11/06" expiration date printed on the tray...

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

Class III — Low RiskOngoing
Refund
DrugJuly 27, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for z-statistic related to...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· JD & SN Inc., dba Moses Lake Professional Pharmacy

Recalled Item: HYDROXOCOBALAMIN (PRESERVATIVE FREE) UNIT DOSE SYRINGES Recalled by JD & SN...

The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray...

The Issue: Defective Delivery System: Inhalers do not spray properly, emitting either...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· Shionogi Inc.

Recalled Item: Nisoldipine Extended Release Tablets Recalled by Shionogi Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJuly 24, 2015· Ucb, Inc

Recalled Item: univasc (moexipril HCl) tablets Recalled by Ucb, Inc Due to Failed...

The Issue: Failed Dissolution Testing: Failed 24 month dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· Teva Pharmaceuticals USA

Recalled Item: ADRUCIL (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Presence of Particulate Matter: silcone rubber and fluorouracil crystals...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2015· JD & SN Inc., dba Moses Lake Professional Pharmacy

Recalled Item: PROGESTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...

The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· JD & SN Inc., dba Moses Lake Professional Pharmacy

Recalled Item: METHIONINE/CHOLINE/INOSITOL Recalled by JD & SN Inc., dba Moses Lake...

The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

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

Class II — Potential Health HazardOngoing
Refund