US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 21, 2017 (9 years ago)

Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol (22 mEq K+) Total…

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

Why it was recalled

Lack of sterility assurance

What was recalled

Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol (22 mEq K+) Total Approximate Volume 255 mL, Rx only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0841-32

Recalling firm
SCA Pharmaceuticals
NDC code
70004-0841-32
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0978-2017

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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