FDAFDA · Food and drugs·Recall number D-097-2013
CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05; b) 120-count capsules per bottle, NDC 0004-0259-51; Made in Ireland; Distributed by: Genentech USA, Inc., South San Francisco, CA 94080.
Published December 26, 2012 · Recall initiated: September 27, 2012
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
Short Fill: some bottles contained less than 120-count per labeled claim.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Genentech, Inc.
- Distributor
- Nationwide
- Lot
- Lot #: a) M1365B01, Exp 04/15; b) M1365, Exp 04/15
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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