February 2019 FDA Recall Drug by Mcguff Compounding Pharmacy Services, Inc.
D-0821-2020 - Presence of Particulate Matter

This Class II drug recall was voluntarily initiated by Mcguff Compounding Pharmacy Services, Inc. on February 14, 2019 for the product Drug. The FDA reported the reason for recall as presence of particulate matter. The product was distributed in Prescriptions filled for patients in the following states: AK, AZ, CA, CO, DC, FL, IN, MA, MT, NC, NJ, NY, OR, SC, TX, UT, VA, WA, and WI. and the recall is currently terminated.

Recall Number: D-0821-2020

Reason for Recall
Presence of Particulate Matter: Particulates observed in vials release for dispensing.
Initiated
02-14-2019
Reported
02-05-2020
Quantity
N/A

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
McGuff Compounding Pharmacy Services, Inc.
Prescriptions filled for patients in the following states: AK, AZ, CA, CO, DC, FL, IN, MA, MT, NC, NJ, NY, OR, SC, TX, UT, VA, WA, and WI.
Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding Pharmacy Services, Inc. Santa Ana, CA 92704

Batch or Lot Expiration Information

Lot# 18J1081, Exp 03/10/19