Home/Recalls/FDA-Z-2596-2026
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ...

Published: July 1, 2026Recall ID: Z-2596-2026Category: devicesCountry: US

Reason for Recall / Hazard

Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.

Product Description & Identification

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. FTMC C-SECTION TRAY-LF DYNJ54603B

Affected Products

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. FTMC C-SECTION TRAY-LF DYNJ54603B

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id99062
Address 13 Lakes Dr
Address 2N/A
Code infoDYNJ54603B UDI-DI 10195327458188 Lot 24ABO124
Postal code60093-2753
Report date20260701
Product typeDevices
Product quantity113, 843 kits
Reason for recallFirm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260227
Initial firm notificationLetter
Center classification date20260625

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI, WY and the country of Barbados.
Official Agency Alert