FDAFDA · Food and drugs·Recall number D-1230-2016
NANDROLONE DEC 200MG/ML W/PRES. (BENZYL ETOH 10%), In a) 2ML Vials, b) 4ML Vials, and c) 5ML Vials, MEDAUS PHARMACY
Published July 20, 2016 · Recall initiated: May 13, 2016
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
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Medaus, Inc.
- Distributor
- U.S. Nationwide, Japan, and New Zealand.
- Lot
- a) Lot #: 160203-18, BUD: 08/01/16. b) Lot #: 160203-18, BUD: 08/01/16. c) Lot #: 160203-18, BUD: 08/01/16.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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