Recall Z-3108-2026— AVID Medical, Inc.

Name: FDA recall Z-3108-2026
Creator: U.S. Food and Drug Administration
Published: 2026-07-14

Class I · Ongoing

Class I FDA medical device recall by AVID Medical, Inc., initiated 2026-07-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard IV START KIT NON-STERILE REF: KRIV26-02. Reason: Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides.

Recalling firm: AVID Medical, Inc.
Classification: Class I
Status: Ongoing
Initiated: 2026-07-14
Firm location: Toano, VA, United States

Product description

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

Reason for recall

Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides

Data sourced from openFDA. This site is unofficial and independent of the FDA.