Home/Recalls/FDA-Z-2417-2026
FDA DevicesClass II

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-...

Published: June 24, 2026Recall ID: Z-2417-2026Category: 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

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G

Affected Products

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98951
Address 13 Lakes Dr
Code infoDYNJ84775A UDI-DI 10195327606527 lot 25LMH070 DYNJ47269D UDI-DI 10195327674786 lot 25LMJ234 DYNJ63276G UDI-DI 10198459458835 lot 26BBC598
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