D-0190-2019 Class II Terminated

Recalled by Pharm D Solutions, LLC — Houston, TX

Recall Details

Product Type
Drugs
Report Date
November 7, 2018
Initiation Date
September 10, 2018
Termination Date
February 5, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
553 vials

Product Description

Tri-Mix XL 150 mg/10 mg/100 mcg a) Injectable NDC 69699-1353-10; b) (LYO) Powder NDC 69699-1353-10, Pharm D Solutions, Houston, Texas

Reason for Recall

Lack of Assurance of Sterility

Distribution Pattern

Nationwide

Code Information

Lot: a) 04132018:97 Discard by: 10/10/2018; 04032018:25 Discard by: 9/30/2018; b) 04162018:29 Discard by: 10/11/2018; 03282018:80 Discard by: 9/24/2018; 06122018:06 Discard by: 12/9/2018; 08132018:55 Discard by: 2/9/2019