US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 5, 2020 (6 years ago)

Sodium Chloride 0.9% Injection, USP, 1000 mL bags, Rx only, Manufactured by: Fresenius…

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

Why it was recalled

CGMP Deviation: Chemical indicators were not positioned properly during sterilization process.

What was recalled

Sodium Chloride 0.9% Injection, USP, 1000 mL bags, Rx only, Manufactured by: Fresenius Medical Care North America, Waltham, MA 02451

Recalling firm
Fresenius Medical Care Holdings, Inc.
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1064-2020

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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