FDAClass IIDecember 24, 2025

Halyard recall

Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.

Why was Halyard recalled?

Potential for incomplete seal on header bag.

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?

Catalog Number: VAST018-10. UDI-DI: 10809160452257. Lot Number: 1651776. Expiration Date: 3/12/2027

Product
Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.
Recalling firm
AVID Medical, Inc.
Quantity
42 units
Distribution
US distribution to GA, IL, NE, MD.
Recall date
December 24, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls