Atlas FDA

Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIA

FDA device recall Z-2424-2026 · posted 2026-06-12 · Open, Classified

Recall details

Recalling firm
Medline Industries, LP
Reason for recall
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Action taken
Firm began notifying consignees on 4/27/2026. Customers were instructed to request stickers to over-label affected convenience kits with a warning label. Warning label indicates for user to remove the affected component and replace it with product from supply. No kits are to be returned.
Root cause
Process control
Status
Open, Classified
Product code
LRO
Quantity affected
49,654 kits total
Distribution
US Nationwide distribution. OUS distribution pending.
Date initiated
2026-04-27
Date posted
2026-06-12
Location
Northfield, IL

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