Class III
Terminated
Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA PHARMACEUTICALS IND. LTD. Jerusalem, 9777402, Israel, Manufactured for: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454, NDC 0093-7440-01.
This recall has been terminated (originally issued August 3, 2016).
- Company
- Teva North America
- Recall Initiated
- May 18, 2016
- Posted
- August 3, 2016
- Recall Number
- D-1449-2016
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 14, 370 units
- Firm Location
- Horsham, PA, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Tablet/Capsule Specifications
Distribution
Nationwide and Puerto Rico
Lot / Code Info
Lot #: 02D163, Exp. 9/2017
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