Lidocaine/Priloc/PE 15/5/0.25% 30 GM jars

FDA Recall #D-0805-2020 — Class II — December 18, 2019

Recall #D-0805-2020 Date: December 18, 2019 Classification: Class II Status: Terminated

Product Description

Lidocaine/Priloc/PE 15/5/0.25% 30 GM jars

Reason for Recall

Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.

Recalling Firm

MPRX, Inc. dba Medical Park Pharmacy — Dallas, TX

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

2 jars

Distribution

TX

Code Information

Lot: 61367:42 Use by: 04/28/2020

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated