US Drug Recall Register
Class I · High risk Terminated Initiated Mar 5, 2015 (12 years ago)

0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc…

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

Why it was recalled

Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.

What was recalled

0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.

Recalling firm
Hospira Inc.
NDC code
0409-7983-25
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0976-2015

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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