Home/Recalls/FDA-Z-2435-2026
FDA DevicesClass II

Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS76...

Published: June 24, 2026Recall ID: Z-2435-2026Category: 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: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K

Affected Products

Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98951
Address 13 Lakes Dr
Code infoDYNJ905154I UDI-DI 10198459549977 lots 26ABB308 26BBA671 CDS760053K UDI-DI 10195327182977 lot 25KBP010
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