Home/Recalls/FDA-Z-1195-2026
FDA DevicesClass II

Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN D...

Published: February 4, 2026Recall ID: Z-1195-2026Category: devicesCountry: US

Reason for Recall / Hazard

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

Product Description & Identification

Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22880; 2) ADULT CVC DRSG CHG W/ADHESIVE, Kit SKU DYNDC3283A.

Affected Products

Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22880; 2) ADULT CVC DRSG CHG W/ADHESIVE, Kit SKU DYNDC3283A.

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98226
Address 13 Lakes Dr
Address 2N/A
Code infoMedline Kit SKU DT22880: UDI/DI 10653160995470 (EA) 40653160995471 (CS), Lot Number 25KMJ441; Medline Kit SKU DYNDC3283A: UDI/DI 10198459313240 (EA) 40198459313241 (CS), Lot Number 25KMH515.
Postal code60093-2753
Report date20260204
Product typeDevices
Product quantity1,928 total
Reason for recallMedline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251212
Initial firm notificationTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date20260128

Overview

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