US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 17, 2023 (3 years ago)

PHENYLephrine in 0.9 sodium chloride, 800 mcg /10 mL, (80 mcg/mL), 10 mL Syringe, Rx…

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

Why it was recalled

Lack of assurance of sterility: Lack of validation data for sanitization cycles

What was recalled

PHENYLephrine in 0.9 sodium chloride, 800 mcg /10 mL, (80 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-6008-1

Recalling firm
Central Admixture Pharmacy Services Inc
NDC code
71286-6008-1
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1077-2023

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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