ROcuronium Bromide 50 mg/ recalled over manufacturing violations
- Recall date
- July 10, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- New England Life Care, Inc. dba Advanced Compounding Solutions recalls ROcuronium Bromide 50 mg/5 mL ( 10 mg/mL), 5mL Syringe, RX Only, Advanced Compounding Solutions, 4 Constitution Way Ste…
- Recall number
- D-0928-2023
- FDA classification
- Class II
- Brand / firm
- New England Life Care, Inc. dba Advanced Compounding Solutions
- Sold / distributed
- Nationwide in the USA
Why it was recalled
CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
ROcuronium Bromide 50 mg/5 mL ( 10 mg/mL), 5mL Syringe, RX Only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042, NDC: 71546-090-05
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