FirstAlerts

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

The FDA has expanded a recall of certain sodium chloride injections distributed across 14 states due to possible fiberglass contamination.

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. ETWritten Aug 27, 2026, 3:22 p.m. ET
The U.S. Food and Drug Administration has expanded a recall of sodium chloride injections made by , according to a report from WNDU. The injections , the FDA reported. as of the report. The recall now includes lot codes Y495523 and Y495523A, according to WNDU. The injections were distributed in . The FDA advises consumers to stop using the affected product immediately and to report any adverse effects through the FDA’s MedWatch reporting program.

Earlier reports

  1. Aug 27, 2026, 3:21 p.m. ET

    FDA Reports Injuries in Baxter Sodium Chloride Injection Recall

    The U.S. Food and Drug Administration (FDA) has received reports of injuries or illnesses associated with Baxter International's recalled sodium chloride injections, according to WNDU. The agency had previously announced the recall of certain lots due to possible fiberglass contamination.

    The recall covers products distributed in Florida, Illinois, Indiana, Louisiana, Maryland, Missouri, North Carolina, New Jersey, Nevada, New York, Ohio, South Carolina, Texas and Virginia. The affected lots are identified by codes Y495523 and Y495523A.

    The FDA advises consumers to stop using the affected product immediately and to report any adverse effects through the agency's MedWatch reporting program. The agency has not specified the nature or severity of the reported injuries or illnesses.

  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 127 Aug 2026, 19:22current

    First published.

  2. Version 127 Aug 2026, 19:16current

    First published.

  3. Version 127 Aug 2026, 19:21current

    First published.

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