Succinylcholine Chloride Injection 20 mg per mL recalled over sterility concerns
- Recall date
- June 26, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- PharMedium Services, Llc recalls Succinylcholine Chloride Injection (Preserved) 20 mg per mL, 200 mg per 10 mL, 10 mL Total Volume in BD Syringe, For IV…
- Recall number
- D-0985-2017
- FDA classification
- Class II
- Brand / firm
- PharMedium Services, Llc
- Sold / distributed
- Nationwide
Why it was recalled
Lack of Assurance of Sterility; media fill failure at manufacturer
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Succinylcholine Chloride Injection (Preserved) 20 mg per mL, 200 mg per 10 mL, 10 mL Total Volume in BD Syringe, For IV Use, PharMedium Services, LLC, Cleveland, MS --- NDC 61553-364-65
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