Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2419-2026Class II

Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT...

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

Medline Industries, LP began a recall of Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C 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-2419-2026
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product
Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C
Product code
OFF Central Venous Catheter 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
DYNDC3525 UDI-DI 10198459576294 Lot 25KBM985 DT13191A UDI-DI 10653160998914 Lot 26AMA168 CDS982047S UDI-DI 10198459385735 Lot 26AMB202 DYNJ62889C UDI-DI 10198459416453 Lot 26AMA584

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2419-2026
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