Pharm D Solutions, LLC recalls 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, H
Recalled November 7, 2018 · FDA recall D-0190-2019 · Pharm D Solutions
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
553 vials
Sold at
Nationwide
Description
Lack of Assurance of Sterility
Product
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
Manufacturer(s)
Pharm D Solutions, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →