Pharm D Solutions, LLC recalls Bi-Mix Injection (Alprostadil 80 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1317-03
Recalled November 7, 2018 · FDA recall D-0143-2019 · Pharm D Solutions
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
115 milliliters
Sold at
Nationwide
Description
Lack of Assurance of Sterility
Product
Bi-Mix Injection (Alprostadil 80 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1317-03
Manufacturer(s)
Pharm D Solutions, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →