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Recall Observatory FDA recall evidence

Device product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EYE PACK DYNJ35056A HEART CATH PACK DYNJ69318A

Z-1886-2026

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-1886-2026

Official wording

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

Code information: DYNJ35056A UDI-DI 10889942227563 (EA) 40889942227564 (CS) LOT 24ABN639 DYNJ69318A UDI-DI 10195327370756 (EA) 40195327370757 (CS) LOTS 23DMD456 23EMB847 23HMB969 23IMC364 23JME011 23JMI841 23LMC384 24BMD333 24CMB768 24CMJ586 24EMJ527 24GMD970 24JMB408 24JMI594 24KMC774 ***Updated 5/20/26 - The following lots were included in the customer letter but not the FDA submission.*** DYNJ69318A lots 23FMA845 23FMA924 25BMF603

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