FirstAlerts

Baxter Sodium Chloride Injection Recalled Over Possible Fiberglass Contamination

The FDA announced a recall of certain lots of 0.9% Sodium Chloride Injection due to potential fiberglass contamination; no injuries have been reported.

3 reports on this incident · first at Aug 27, 2026, 3:16 p.m. ET

By AI ReporterFirst reported Aug 27, 2026, 3:02 p.m. ETUpdated Aug 28, 2026, 4:11 p.m. ET
The U.S. Food and Drug Administration (FDA) announced a recall of certain lots of made by , according to WNDU and biztoc.com. The recall was reported on August 28, 2026. The reason for the recall is conflicting: biztoc.com reports the in the solution, while WNDU reports the product . , according to WNDU. The affected lots are identified by codes Y495523 and Y495523A, according to WNDU. The distribution is also conflicting: WNDU reports the recall covers , while biztoc.com reports the recall is . The FDA advises consumers to stop using the affected product immediately and to report any adverse effects through the FDA's MedWatch reporting program, according to WNDU.

Earlier reports

  1. Aug 27, 2026, 3:22 p.m. ET

    FDA Expands Recall of Baxter Sodium Chloride Injections Over Possible Fiberglass Contamination

    The U.S. Food and Drug Administration has expanded a recall of sodium chloride injections made by Baxter International, according to a report from WNDU. The injections may be contaminated with fiberglass, the FDA reported. No injuries or illnesses had been reported as of the report.

    The recall now includes lot codes Y495523 and Y495523A, according to WNDU. The injections were distributed in Florida, Illinois, Indiana, Louisiana, Maryland, Missouri, North Carolina, New Jersey, Nevada, New York, Ohio, South Carolina, Texas and Virginia.

    The FDA advises consumers to stop using the affected product immediately and to report any adverse effects through the FDA’s MedWatch reporting program.

  2. Aug 27, 2026, 3:16 p.m. ETFirst report

    Sodium Chloride Injections Recalled Over Possible Fiberglass Contamination

    Baxter International is recalling certain sodium chloride injections that may be contaminated with fiberglass, according to a report from WNDU.com. The recall affects product codes Y495523 and Y495523A, distributed in Florida, Illinois, Indiana, Louisiana, Maryland, Missouri, North Carolina, New Jersey, Nevada, New York, Ohio, South Carolina, Texas and Virginia.

    The U.S. Food and Drug Administration (FDA) announced the recall, advising consumers to stop using the affected product immediately and to report any adverse effects through the FDA's MedWatch reporting program. As of the report, no injuries or illnesses had been reported.

    The recall was reported on August 27, 2026.

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Revision history

  1. Version 228 Aug 2026, 20:11current

    Corrected to state no injuries reported, added conflicting distribution and reason details, and removed unverified injury reports.

  2. Version 127 Aug 2026, 19:22current

    First published.

  3. Version 127 Aug 2026, 19:16current

    First published.

  4. Version 127 Aug 2026, 19:21

    First published.

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