US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 24, 2015 (11 years ago)

DMPS (DIMERCAPTO-PROPANESULFONIC NA (SINGLE USE ONLY), Injectable Solution, 500 mg/mL…

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

Why it was recalled

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

What was recalled

DMPS (DIMERCAPTO-PROPANESULFONIC NA (SINGLE USE ONLY), Injectable Solution, 500 mg/mL, 5mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Recalling firm
JD & SN Inc., dba Moses Lake Professional Pharmacy
Origin
WA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0076-2016

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.