Drug recall D-1041-2018
Product
Diazepam Rectal Gel, 2.5 mg, TWIN PACK that Contains two pre-filled, unit-dose, rectal delivery systems with lubricating jelly and instructions for use per carton, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807; Manufactured by: DPT Laboratories, Ltd., San Antonio, TX 78215; NDC 68682-650-20.
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.
Lots and codes
Lot #: NBBN, Exp 02/22
Recall details
- Recalling firm
- Valeant Pharmaceuticals North America LLC, Bridgewater, NJ
- Quantity
- 306 cartons
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 10, 2018
- Terminated
- February 5, 2019
Related products
- Diazepam – drug information
- NDC 68682-650 Diazepam · Diazepam 2.5 mg/.5mL · Oceanside Pharmaceuticals
- NDC 68682-652 Diazepam · Diazepam 10 mg/2mL · Oceanside Pharmaceuticals
- NDC 68682-655 Diazepam · Diazepam 20 mg/4mL · Oceanside Pharmaceuticals