FDAFDA · Food and drugs·Recall number D-579-2013
Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET Solutions, Inc., Knoxville, TN
Published June 12, 2013 · Recall initiated: February 22, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
cGMP Deviation
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Petnet Solution Inc
- Distributor
- Within the state of CA.
- Lot
- 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]
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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