Baxter Issues Voluntary Nationwide Recall For Two Lots Of 0.9% Sodium Chloride Injection Due To Potential Presence Of Particulate Matter

Recall Summary Baxter is recalling two lots of 0.9% Sodium Chloride Injection because fiberglass particles may be present in the solution. This product is an injectable saline solution used in medical settings. The recall affects patients who received injections from the affected lots.

Recalling firm

Baxter

Product

for Two Lots of 0.9% Sodium Chloride Injection

Reason

FOR IMMEDIATE RELEASE – AUG. 25, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling two lots of 0.9% Sodium Chloride Injection due to the potential presence of particulate matter identified as fiberglass in the solution.

Category

drug recall

Country

United States

Agency

FDA-MEDWATCH-RSS

Recall date

2026-08-26

Status

Ongoing

Official recall notice from FDA-MEDWATCH-RSS

Recall details on Nibble Recalls: https://trynibble.app/recalls/34215116-c0a1-4e05-b579-5af0c57465d4