2% Lidocaine HCl Injectable Solution recalled over sterility concerns
- Recall date
- March 13, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Advanced Pharma Inc. recalls 2% Lidocaine HCl Injectable Solution, 60 mg/3 mL (20 mg per mL), 3mL Sterile single use syringe, NDC: 42852-011-22 Avel…
- Recall number
- D-1026-2019
- FDA classification
- Class II
- Brand / firm
- Advanced Pharma Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Lack of Assurance of Sterility
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
2% Lidocaine HCl Injectable Solution, 60 mg/3 mL (20 mg per mL), 3mL Sterile single use syringe, NDC: 42852-011-22 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Get recall alerts
Free email alert whenever Advanced Pharma Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Advanced Pharma Inc.