TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEU...

FDA Recall #D-0326-2017 — Class III — December 22, 2016

Recall #D-0326-2017 Date: December 22, 2016 Classification: Class III Status: Terminated

Product Description

TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21

Reason for Recall

Failed Stability Specifications

Recalling Firm

Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals — Huntsville, AL

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

1200 bottles

Distribution

Nationwide

Code Information

T248H15A, Exp. 08/17

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated