Class III
Terminated
Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
This recall has been terminated (originally issued January 25, 2017).
- Company
- Teva Pharmaceuticals Usa
- Recall Initiated
- December 1, 2016
- Posted
- January 25, 2017
- Recall Number
- D-0431-2017
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 6,800 cartons
- Firm Location
- North Wales, PA, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Dissolution Specifications
Distribution
Nationwide in the USA and Puerto Rico
Lot / Code Info
Lot # 34027040A; Exp 10/17
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