Home / Recalls / Valeant Pharmaceuticals North America LLC / D-1041-2018

D-1041-2018 Class III Terminated

Recalled by Valeant Pharmaceuticals North America LLC — Bridgewater, NJ

Recall Details

Product Type
Drugs
Report Date
August 15, 2018
Initiation Date
July 10, 2018
Termination Date
February 5, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
306 cartons

Product Description

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.

Distribution Pattern

Nationwide in the USA

Code Information

Lot #: NBBN, Exp 02/22

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