D-579-2013 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- June 12, 2013
- Initiation Date
- February 22, 2013
- Termination Date
- June 6, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 28 doses
Product Description
Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET Solutions, Inc., Knoxville, TN
Reason for Recall
cGMP Deviation
Distribution Pattern
Within the state of CA.
Code Information
Batch # BN-3350 Rx #s: [38126044] [38126058] [38126059] [38126021] [38126022] [38126023] [38125981] [38125991] [38125992] [38126016] [38126017] [38126004] [38126005] [38126006] [38126007] [38126057] [38125999] [38126036] [38126037] [38126038] [38125998] [38126033]