FDA recall D-0145-2017

Product

Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria, NDC 0409-7332-01

Reason for recall

Labeling: Missing Label

Distribution

WI

Key facts

Status

Terminated

Initiation date

2016-10-19

Report date

2016-11-30

Termination date

2017-07-27

Voluntary/Mandated

Voluntary: Firm initiated

Location

Princeton, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0145-2017