FDA recall D-0132-2018

Product

HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-165-78

Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp. Date

Distribution

Nationwide.

Key facts

Status

Terminated

Initiation date

2017-09-26

Report date

2018-01-03

Termination date

2020-05-19

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0132-2018