FDAClass IIJune 24, 2026

Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D recall

Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D

Why was Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D recalled?

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

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?

UDI-DI 10198459409431 Lot 25KBB755

Product
Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total
Distribution
US Nationwide distribution. OUS distribution pending.
Recall date
June 24, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls