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Class IOngoing

AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE REF: KRIV26-02

Recall date · record updated Sep 23, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
AVID Medical, Inc.
Reason
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
Hazard
FDA Class I: a reasonable probability that use or exposure will cause serious adverse health consequences or death (FDA definition).
Who’s affected
US Nationwide distribution in the state of NE.
Where
Nationwide
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99672…

Products

  1. Halyard IV START KIT NON-STERILE REF: KRIV26-02

    Codes/lots: Lot Number: 1658437 UDI: 10809160460481Quantity: 288 unitsRecall no. Z-3108-2026Class I

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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