Lidocaine/Priloc/PE 30/5/0.25% 30 GM jars
FDA Recall #D-0806-2020 — Class II — December 18, 2019
Product Description
Lidocaine/Priloc/PE 30/5/0.25% 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
12 jars
Distribution
TX
Code Information
Lots: 61134:42 Use by: 01/31/2020; 61302:26 Use by: 04/14/2020; 61318:42 Use by: 04/19/2020
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated