Home/Recalls/FDA-Z-2440-2026
FDA DevicesClass II

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING...

Published: June 24, 2026Recall ID: Z-2440-2026Category: devicesCountry: US

Reason for Recall / Hazard

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

Product Description & Identification

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A

Affected Products

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98951
Address 13 Lakes Dr
Code infoEBSI1688 UDI-DI 10653160370130 Lot 2025102890 EBSI1328A UDI-DI 10653160382980 Lot 2025103090
Postal code60093-2753
Report date20260624
Product typeDevices
Product quantity49,654 kits total
Reason for recallKits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260427
Initial firm notificationTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date20260612

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution. OUS distribution pending.
Official Agency Alert