Class II
Terminated
Actiq (oral transmucosal fentanyl citrate) 200 mcg, lozenge on a stick, a)Single Blister (NDC 63459-502-01), b) 30 count carton (NDC 63459-502-30), Rx only, Manufactured by: Cephalon, Inc., Salt Lake City, UT 84116
This recall has been terminated (originally issued June 26, 2013).
- Company
- Teva Pharmaceuticals Usa, Inc.
- Recall Initiated
- May 28, 2013
- Posted
- June 26, 2013
- Recall Number
- D-606-2013
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 316 cartons
- Firm Location
- Sellersville, PA, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Dissolution Specification; during stability testing
Distribution
Product was distributed within the United States to FL, IL, MA, MO, MS, OH and TX. No government or foreign distribution.
Lot / Code Info
Lot C88583, exp. 06/15
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