Heritage Pharmaceuticals, Inc. recalls Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceutical…
- Recall date
- February 15, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1065-2019
- FDA classification
- Class II
- Brand / firm
- Heritage Pharmaceuticals, Inc.
- Sold / distributed
- Nationwide within the United States
Why it was recalled
Subpotent Drug.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31
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