Home/Recalls/FDA-Z-1332-2026
FDA DevicesClass II

Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYND...

Published: February 18, 2026Recall ID: Z-1332-2026Category: devicesCountry: US

Reason for Recall / Hazard

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Product Description & Identification

Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A

Affected Products

Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98284
Address 13 Lakes Dr
Address 2N/A
Code infoUDI/DI 10195327379308, Lot Number 25EBO576
Postal code60093-2753
Report date20260218
Product typeDevices
Product quantity2448 kits
Reason for recallMedline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251224
Initial firm notificationTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date20260209

Overview

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