FirstAlerts

FDA Reports Injuries in Avid Medical IV Start Kit Fungal Contamination Issue

The FDA says Avid Medical has reported injuries associated with the fungal contamination issue affecting certain convenience kits.

3 reports on this incident · first at Aug 31, 2026, 10:39 p.m. ET

By AI ReporterFirst reported Aug 28, 2026, 12:00 a.m. ETWritten Aug 31, 2026, 11:23 p.m. ET
The U.S. Food and Drug Administration (FDA) reports that has now reported injuries associated with the fungal contamination issue affecting certain IV start kits. As of August 20, the agency states that has not reported any serious injuries or deaths associated with this issue, but injuries have been reported. The FDA issued an early alert on August 28, 2026, regarding , identified by codes AVID KIT KRIV26-02, 1658437, and 10809160460481. The issue involves . The FDA states that certain convenience kits containing recalled BD ChloraPrep applicators should be removed from use due to this contamination. The FDA advises users to review inventory for affected convenience kits, quarantine them, and destroy the entire kit after completion of response forms. The status of the action is .

Earlier reports

  1. Aug 31, 2026, 10:53 p.m. ET

    FDA Closes Recall Action on Avid Medical IV Start Kits Over Fungal Contamination

    The U.S. Food and Drug Administration has closed its recall action on certain Avid Medical IV Start Kits, meaning the agency considers the recall carried out. The action, first announced in an early alert, concerns convenience kits containing recalled BD ChloraPrep applicators that may be contaminated with Aspergillus penicillioides under certain environmental conditions.

    Affected products are identified as AVID KIT KRIV26-02, with codes 1658437 and 10809160460481. As of August 20, Avid Medical had not reported any serious injuries or deaths associated with the issue, according to the FDA.

    The FDA advises anyone still holding affected kits to review inventory, quarantine, and destroy the entire kit after completing response forms.

  2. Aug 31, 2026, 10:39 p.m. ETFirst report

    FDA Issues Early Alert on Avid Medical IV Start Kits Over Fungal Contamination Risk

    The U.S. Food and Drug Administration (FDA) has issued an early alert regarding certain IV start kits distributed by Avid Medical, citing a risk of fungal contamination. According to the FDA, the kits may allow the growth of Aspergillus penicillioides under certain environmental conditions. The affected products are identified as AVID KIT KRIV26-02, with codes 1658437 and 10809160460481, described as "IV START KIT NON-STERILE, KIT."

    The FDA states that the issue involves convenience kits containing recalled BD ChloraPrep applicators, which should be removed from use. As of August 20, Avid Medical has not reported any serious injuries or deaths associated with this issue, according to the FDA. The agency advises healthcare providers to review inventory for affected convenience kits, quarantine them, and destroy the entire kit after completing response forms. The status of the alert is ongoing.

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Revision history

  1. Version 11 Sept 2026, 02:39current

    First published.

  2. Version 11 Sept 2026, 03:23current

    First published.

  3. Version 11 Sept 2026, 02:53current

    First published.

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