Levothyroxine Sodium 325mcg/Ml (0.325mg/Ml) Injectable 15 Ml (1 Product)

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012. FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.

What was recalled

LEVOTHYROXINE SODIUM 325MCG/ML (0.325MG/ML) INJECTABLE 15 ML (1 PRODUCT)

Recalling firm: Franck's Lab Inc., d.b.a. Franck's Compounding Lab
Origin: FL, United States
Initiated by: Voluntary: Firm initiated
FDA recall number: D-1557-2012

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.