Petnet Solution Inc recalls Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET Solutio

Recalled June 12, 2013 · FDA recall D-579-2013 · Petnet Solution

Hazard

cGMP Deviation · FDA Class II

Units

28 doses

Sold at

Within the state of CA.

Description

cGMP Deviation

Product

Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET Solutions, Inc., Knoxville, TN

Manufacturer(s)

Petnet Solution Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →