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Recall Observatory FDA recall evidence

Device product

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIOGRAM PACK-LF DYNJ21574J JUDKINS PACK DYNJ51126

Z-2581-2026

February 27, 2026

Class II

Product summary

Firm
Medline Industries, LP
Event
Event 99062
Status
Ongoing
Classification
Class II
Quantity
113,843 kits
Official record key
device-enforcement:Z-2581-2026

Official wording

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

Code information: DYNJ21574J UDI-DI 10889942153497 Lots 21ALA586 21CLA398 21ELA408 21FLA144 21FLA788 21HLA420 21ILA431 DYNJ51126 UDI-DI 10889942122820 Lots 21ADA917

Distribution pattern: US 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.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    unapproved design changes