US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 14, 2013 (13 years ago)

All Compounded Products, packaged in plastic infusion bags, devices, syringes and glass…

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

Why it was recalled

Lack of Assurance of Sterility; potential for mold contamination

What was recalled

All Compounded Products, packaged in plastic infusion bags, devices, syringes and glass vials, Med Prep Consulting Inc., Tinton Falls, NJ 07712

Recalling firm
Med Prep Consulting, Inc.
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-811-2013

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.