Medical device recalls Moderate risk

Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B ANGIO…

Recall date
February 27, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1884-2026
FDA classification
Class II
Brand / firm
Medline Industries, LP
Sold / distributed
Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B ANGIO PHC DYNJ37485C C.I.C.N. ANGIO PACK DYNJ53064B FHT P NEURO PACK DYNJ39931D NEURO ARTERIOGRAM PACK-LF DYNJ0948060F NEURO KIT NAM0003 NEURO PACK DYNJ61542D NEURO RADIOLOGY PACK DYNJ59903B NEURO TRAY DYNJ84872A PK, CATH LAB-ANGIO DYNJ44027F QVH IR NEURO PACK DYNJ62176

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