US Drug Recall Register
Class I · High risk Terminated Initiated May 12, 2014 (12 years ago)

0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter…

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

Why it was recalled

Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes

What was recalled

0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015

Recalling firm
Baxter Healthcare Corp.
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1550-2014

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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