Alprostadil 2000 mcg/ml (Olympia Pharmacy) – sterility problem (2013)
Class II: 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
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Alprostadil 2000 mcg/ml, compounded by Olympia Pharmacy, Orlando, FL
Brand
Lowlite Investments, Inc. D/B/A Olympia Pharmacy
Lot Codes / Batch Numbers
B5008 exp 12/31/13, K5030 Exp. 11/30/13, A5716 Exp. 8/31/13, C5121 Exp 9/12/13, and C5208 Exp 9/7/13
Products Sold
B5008 exp 12/31/13, K5030 Exp. 11/30/13, A5716 Exp. 8/31/13, C5121 Exp 9/12/13, and C5208 Exp 9/7/13
Lowlite Investments, Inc. D/B/A Olympia Pharmacy is recalling Alprostadil 2000 mcg/ml, compounded by Olympia Pharmacy, Orlando, FL due to Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 7, 2026