Home/Recalls/FDA-Z-2416-2026
FDA DevicesClass II

BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A

Published: June 24, 2026Recall ID: Z-2416-2026Category: 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

BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A

Affected Products

BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98951
Address 13 Lakes Dr
Code infoDYNJRA2119A UDI-DI 10198459194702 lot 25LBB738 DYNJRA1011A UDI-DI 10888277783614 lots 25KBB849 25LBB734
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