March 2020 FDA Recall Drug by Jubilant Draximage Inc
D-1062-2020 - Failed Stability Specifications

This Class II drug recall was voluntarily initiated by Jubilant Draximage Inc on March 19, 2020 for the product Drug. The FDA reported the reason for recall as failed stability specifications. The product was distributed in Product was distributed throughout the United States. and the recall is currently terminated.

Recall Number: D-1062-2020

Reason for Recall
Failed Stability Specifications
Initiated
03-19-2020
Reported
04-01-2020
Quantity
473 kits of 30 vials

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
85226
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Jubilant Draximage Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Product was distributed throughout the United States.
Termination Date About Termination Date
Date that FDA officially terminated the recall.
05-19-2021
Product Description About Product Description
Full technical description of the product.
DRAXIMAGE DTPA (KIT FOR THE PREPARATION OF TECHNETIUM TC 99M PENTETATE INJECTION), 20 mg vial, Rx only, Manufactured for: Jubilant Draximage, Inc., Kirkland, Quebec, Canada, NDC 65174-288-05, 67175-288-30

Batch or Lot Expiration Information

Lot# 8K143, Exp 10/31/2020.