US Drug Recall Register
Class I · High risk Terminated Initiated Aug 31, 2012 (14 years ago)

0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter; product may contain fibrous material

What was recalled

0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23

Recalling firm
Hospira Inc.
NDC code
0409-7984-23
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-922-2013

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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