D-0763-2020 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- January 22, 2020
- Initiation Date
- December 20, 2019
- Termination Date
- October 27, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5 vials
Product Description
QUADMIX in 1 mL vial Assurance Infusion (713)-533-8800
Reason for Recall
Lack of sterility assurance.
Distribution Pattern
Nationwide within the United States
Code Information
Lot: 07012019@30 Exp. 12/28/2019