US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 7, 2017 (9 years ago)

Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total…

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

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.

What was recalled

Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0600-12

Recalling firm
SCA Pharmaceuticals
NDC code
70004-0600-12
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0156-2018

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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