FDA alerts users to destroy AVID Medical IV start kits containing recalled BD ChloraPrep applicators due to fungal contamination risk

The FDA's Center for Devices and Radiological Health issued an Early Alert warning that certain AVID Medical convenience kits may pose a high‑risk fungal contamination problem because they contain a recalled BD ChloraPrep applicator.

The affected product is the non‑sterile IV START KIT (model KRIV26‑02, lot 1658437) identified by its unique device identifier. The agency advises users to remove these kits from inventory and cease any further use.

AVID Medical sent a letter on August 18 directing customers to quarantine and destroy the entire kit, replacing an earlier July 14 notice that had only required over‑labeling and removal of the contaminated component at the point of use.

Facilities should review their stock, complete the required response forms, and follow the destruction instructions to eliminate the potential contamination risk.