Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 — Class I medical device recall Z-2444-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-08-14, distributed nationwide. Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. L

Recall number	`Z-2444-2024`
Product type	Medical device
Classification	Class I
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated	2024-04-08
Classified	2024-08-08
Reported by FDA	2024-08-14
Distributed	Nationwide (US)
Quantity	1,679,067 units
Reason classes	packaging, device malfunction
Lot numbers	`21IBX266`, `21KBH003`, `22DBD158`, `22FBD709`, `22FBY433`, `22GBH459`, `22GBK576`, `22GBN555`, `22HBQ139`, `22HBR225`, `22IBJ562`, `22IBO303`, `22JBO861`, `22JBP469`, `22JBQ914`, `23ABM365`, `23ABN207`, `23ABT952`, `23BLA187`, `23CBF157`, `23CBM109`, `23DBN340`, `23DLA246`, `23EBE461`, `23EBI477`, `23FBR368`, `23GBH016`, `23HBD973`, `23HBK882`, `23HBN396`, `23IBD357`, `23IBS867`, `23KLA117`, `23KMB066`, `23LLA329`, `24ABN950`, `24ABO025`, `CMPJ11455B`, `DYNJ26938J`, `DYNJ49920L` and 7 more

Product

Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack Number CMPJ11455B ; 3) SALEM CATH LAB-LF , Pack Number DYNJ26938J ; 4) EH PEDIATRIC CATH , Pack Number DYNJ49920L ; 5) ARTERIOGRAM PACK, Pack Number DYNJ53018; 6) CATH PACK , Pack Number DYNJ57729C ; 7) PEDS CATH PACK, Pack Number DYNJ66856; 8) PEDS CATH PACK, Pack Number DYNJ66856A ; 9) STEWARD ROCKLEDGE CATH RRS, Pack Number DYNJ81061A ; 10) CATH LAB PACK , Pack Number DYNJ84617; 11) UA/UV CATHETERIZATION TRAY, Pack Number UVT1190A

Reason for recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2444-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.