US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 26, 2017 (9 years ago)

0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira…

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

Why it was recalled

Presence of Particulate Matter; stainless steel

What was recalled

0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09

Recalling firm
ICU Medical Inc
NDC code
0409-7983-09
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1091-2017

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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