FDA recall record

SODIUM CHLORIDE 0.9% Sodium Chloride Injection USP, 500 mL recall — FDA D-0491-2025

Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.

Class IIclassification
D-0491-2025official record ID
Jul 2, 2025report date

Recall record at a glance

Official recordD-0491-2025
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmB BRAUN MEDICAL INC
Report dateJul 2, 2025
Recall initiation dateJun 16, 2025
Quantity187,656 containers
LocationAllentown, PA, United States

Official product description

0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and further packaged 24 per case, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC 0264-7800-10.

Why the product was recalled

Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.

Distribution information

USA Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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