FDAClass IRecall started July 22, 2026

Halyard IV Start KIT Non-Sterile Recall: Contamination

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

Why was Halyard IV Start KIT Non-Sterile recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Kit Model Number: KRIV26-02. UDI-DI: 10809160460481. Lot Number: 1658437. Expiration Date: 1/31/2027

Product
Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02.
Recalling firm
AVID Medical, Inc.
Quantity
288 kits (6 cases)
Distribution
US Nationwide distribution.
Recall started
July 22, 2026
Report date
September 30, 2026
Classification
Class I
Status
Ongoing
Agency
FDA (device)
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