FDA recall D-0254-2015

Product

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045, NDC 0409-6533-01.

Reason for recall

Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.

Distribution

Nationwide.

Key facts

Status

Terminated

Initiation date

2014-11-07

Report date

2014-11-26

Termination date

2017-03-22

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0254-2015