US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 21, 2015 (11 years ago)

Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Refills (Racepinephrine…

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

Why it was recalled

Discoloration

What was recalled

Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Refills (Racepinephrine USP 11.25 mg), 30 individual foil wrapped vials per carton, Manufactured By: nephron pharmaceuticals corporation, Orlando, FL --- NDC 0487-2784-01

Recalling firm
Nephron Pharmaceuticals Corp.
NDC code
0487-2784-01
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0389-2016

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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