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FDAFDA · Food and drugs·Recall number D-0977-2017

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 70004-0841-40

Published July 19, 2017 · Recall initiated: June 21, 2017

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Lack of sterility assurance

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
SCA Pharmaceuticals
Distributor
LA, PA, NY, WI
Lot
Lot #: 20170509@6, Exp 6/23/2017; 20170519@35, Exp 7/3/2017; 20170523@22, Exp 7/7/2017; 20170525@9, Exp 7/9/2017; 20170605@49, Exp 7/20/2017; 20170605@9, Exp 7/20/2017
Risk classification
Class II
Area (FDA)
drug
Country
United States

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