Lidocaine HCl 1% - Phenylephrine HCl 1 recalled over sterility concerns
- Recall date
- September 20, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Leiter's Compounding recalls Lidocaine HCl 1% - Phenylephrine HCl 1.5% in Sterile Water for Injection (Injection) 1 mL Total Volume in a 2 mL Vial (…
- Recall number
- D-0014-2017
- FDA classification
- Class II
- Brand / firm
- Leiter's Compounding
- Sold / distributed
- Nationwide
Why it was recalled
Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Lidocaine HCl 1% - Phenylephrine HCl 1.5% in Sterile Water for Injection (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-002-35
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