Westlab Pharmacy, Inc. dba Westlab Pharmacy recalls Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00
- Recall date
- August 10, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0089-2019
- FDA classification
- Class II
- Brand / firm
- Westlab Pharmacy, Inc. dba Westlab Pharmacy
- Sold / distributed
- Nationwide
Why it was recalled
Incorrect Product Formulation
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00
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