US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 20, 2018 (8 years ago)

fentanyl Citrate USP 5 mcg in 0.9% Sodium Chloride USP 0.5 mL, 10 mcg per mL prefilled…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent Drug: final drug concentration is subpotent as compared to the concentration indicated on the label.

What was recalled

fentanyl Citrate USP 5 mcg in 0.9% Sodium Chloride USP 0.5 mL, 10 mcg per mL prefilled syringe, Rx only, Advanced Pharma an FDA Regulated 503B Outsourcing Facility 9265 Kirby Dr., Houston, TX 77054, NDC 15082-210-72.

Recalling firm
Advanced Pharma Inc.
NDC code
15082-210-72
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0889-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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