Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2439-2026Class II

Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX...

MEDLINE INDUSTRIES, LP - Northfield / initiated 2026-04-27 / Open, Classified / root cause: manufacturing process

Medline Industries, LP began a recall of Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX PI CVC 7F, 3L, 20CM BUNDLE ECVC6915A ECVC6985B on . FDA classified it as Class II and gives the reason as "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application". As of , the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-2439-2026
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product
Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX PI CVC 7F, 3L, 20CM BUNDLE ECVC6915A ECVC6985B
Product code
LRO General Surgery Tray
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.
Root cause tag
manufacturing process
FDA root cause
Process control
Action
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.
Quantity in commerce
49,654 kits total
Distribution
US Nationwide distribution. OUS distribution pending.
Product codes and lots
ECVC6805B UDI-DI 10653160387428 Lot 2025120890 ECVC8055A UDI-DI 10653160387848 Lot 2025112690 ECVC6915A UDI-DI 10653160389439 Lot 2025102790 ECVC6985B UDI-DI 10653160388272 Lot 2025103190

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2439-2026
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2414-2026Class IIOngoingVoluntary: Firm initiated
Z-2415-2026Class IIOngoingVoluntary: Firm initiated
Z-2416-2026Class IIOngoingVoluntary: Firm initiated
Z-2417-2026Class IIOngoingVoluntary: Firm initiated
Z-2418-2026Class IIOngoingVoluntary: Firm initiated
Z-2419-2026Class IIOngoingVoluntary: Firm initiated
Z-2420-2026Class IIOngoingVoluntary: Firm initiated
Z-2421-2026Class IIOngoingVoluntary: Firm initiated
Z-2422-2026Class IIOngoingVoluntary: Firm initiated
Z-2423-2026Class IIOngoingVoluntary: Firm initiated
Z-2424-2026Class IIOngoingVoluntary: Firm initiated
Z-2425-2026Class IIOngoingVoluntary: Firm initiated
Z-2426-2026Class IIOngoingVoluntary: Firm initiated
Z-2427-2026Class IIOngoingVoluntary: Firm initiated
Z-2428-2026Class IIOngoingVoluntary: Firm initiated
Z-2429-2026Class IIOngoingVoluntary: Firm initiated
Z-2430-2026Class IIOngoingVoluntary: Firm initiated
Z-2431-2026Class IIOngoingVoluntary: Firm initiated
Z-2432-2026Class IIOngoingVoluntary: Firm initiated
Z-2433-2026Class IIOngoingVoluntary: Firm initiated
Z-2434-2026Class IIOngoingVoluntary: Firm initiated
Z-2435-2026Class IIOngoingVoluntary: Firm initiated
Z-2436-2026Class IIOngoingVoluntary: Firm initiated
Z-2437-2026Class IIOngoingVoluntary: Firm initiated
Z-2438-2026Class IIOngoingVoluntary: Firm initiated
Z-2439-2026Class IIOngoingVoluntary: Firm initiated
Z-2440-2026Class IIOngoingVoluntary: Firm initiated
Z-2441-2026Class IIOngoingVoluntary: Firm initiated
Z-2442-2026Class IIOngoingVoluntary: Firm initiated
Z-2443-2026Class IIOngoingVoluntary: Firm initiated
Z-2444-2026Class IIOngoingVoluntary: Firm initiated
Z-2445-2026Class IIOngoingVoluntary: Firm initiated
Z-2446-2026Class IIOngoingVoluntary: Firm initiated
Z-2447-2026Class IIOngoingVoluntary: Firm initiated