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Recall Observatory FDA recall evidence

Device product

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

Z-1885-2026

February 27, 2026

Class II

Product summary

Firm
Medline Industries, LP
Event
Event 98601
Status
Ongoing
Classification
Class II
Quantity
270,311 total
Official record key
device-enforcement:Z-1885-2026

Official wording

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

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

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

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Unapproved design changes