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Recall Observatory FDA recall evidence

Device product

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR G'S BREAST PACK DYNJ51124B LIPO SUPPLEMENT PACK-LF DYNJ0341174D PLASTIC PACK DYNJ66746 DYNJ85702

Z-2584-2026

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-2584-2026

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: DYNJ51124B UDI-DI 10193489579291 Lot 24ABS353 DYNJ0341174D UDI-DI 10195327437749 Lot 24BBB383 DYNJ66746 UDI-DI 10193489375527 Lot 24BBD114 DYNJ85702 UDI-DI 10195327536213 Lot 24ABP053

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