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FDA · Medical devices ·

Halyard IV START KIT NON-STERILE; 48 kits per case recall

AVID Medical, Inc. recalled Halyard IV START KIT NON-STERILE; 48 kits per case on September 30, 2026 because of convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides. It was sold nationwide.

Why it was recalled

Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.

What's recalled

Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02.

Quantity: 288 kits (6 cases)

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
AVID Medical, Inc., Toano, VA
Date
Severity
Class I · most serious
the most serious: the product could cause serious health problems or death.
Where sold
Nationwide
US Nationwide distribution.
Status
Ongoing
Recall number
Z-3194-2026
Source
U.S. Food and Drug Administration

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