Z-1885-2026 Class II Ongoing

Recalled by Medline Industries, LP — Northfield, IL

Recall Details

Product Type
Devices
Report Date
April 29, 2026
Initiation Date
February 27, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
270,311 total

Product Description

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ909398A ROBOTIC PACK DYNJ908706D

Reason for Recall

Unapproved design changes to the products outside of the 510(k) clearance.

Distribution Pattern

Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.

Code Information

DYNJ909398A UDI-DI 10195327338190 (EA) 40195327338191 (CS) LOTS 24GMH510 24HMG886 DYNJ908706D UDI-DI 10198459017773 (EA) 40198459017774 (CS) LOTS 24HMA783 24HMG308 24KMC651 24KMJ274 24LME931 25AME217 25BMI653 ***Updated 5/20/26 - The following lots were included in the customer letter but not in the FDA submission.*** DYNJ909398A lots 23EMF078 23HME512 23HMI269 23JMB528 23KME175 24EMC327