FDAFDA · Food and drugs·Recall number D-1041-2018
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.
Published August 15, 2018 · Recall initiated: July 10, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DIAZEPAM
- Manufacturer
- Valeant Pharmaceuticals North America LLC
- Distributor
- Nationwide in the USA
- Lot
- Lot #: NBBN, Exp 02/22
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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