Convenience kits containing select SKUs of 10mL Polycarbonate Colored… — Class II medical device recall Z-2585-2026
Ongoing recall by Medline Industries, LP, reported 2026-07-01, distributed nationwide. Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products n
| Recall number | Z-2585-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-02-27 |
| Classified | 2026-06-25 |
| Reported by FDA | 2026-07-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | BB |
| Quantity | 113,843 kits |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 10193489345230, 10193489345377, 10193489352375, 10193489397482, 10193489409536, 10193489459081, 10193489472516, 10193489520279, 10193489569827, 10193489688863, 10193489872002, 10193489883596, 10193489925067, 10195327044138, 10195327096991, 10195327406042, 10884389898826, 10888277740273, 10888277762886, 10889942249398, 10889942727919, 10889942777792, 10889942893645, 10889942925421, 10889942952977 |
| Lot numbers | 00-402001S, 21ABP630, 21ABV063, 21ABV982, 21BBE987, 21BBK296, 21BDA459, 21BDA985, 21BDB242, 21BDB710, 21BMB700, 21CBA985, 21CBB916, 21CBX170, 21CDA191, 21CDA233, 21CDC063, 21CDC092, 21CMA789, 21DBD058, 21DBL459, 21DBU969, 21DDA549, 21DDB648, 21DDB799, 21DDB919, 21EBC916, 21EBD905, 21EDA769, 21EDC220, 21FBF623, 21FBK360, 21FBN495, 21FMF068, 21GBG636, 21GBQ837, 21GDB289, 21GDC682, 21GDC975, 21GDD035 and 131 more |
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. AAA DYNJ905651B ARTERIOGRAM TRAY 00-402001S AV SHUNT PACK-LF DYNJ0842516F BASIC IR PACK-LF PHS463660F CATH PROCEDURAL TRAY DYNJ43580C CONGENITAL ADD-ON KIT DYNDA2213A CUSTOM PROCEDURE KIT DYNJ65277A DEEP BRAIN STIMULATION PACK DYNJ0842793F HOSPITAL REGIONAL DE CONCEPCIO DYNJ67918 INTERVENTIONAL PACK DYNJ56666B INVASIVE LINE INSERTION DYNJ44123A JUDKINS PACK DYNJ51126B LARKIN CUSTOM NEURO TRAY PAIN1454 MAJOR PLUS PACK DYNJ905160I MINIMALLY INVASIVE PACK-LF DYNJ0843063J NEURO ANGIO PACK SJF-LF DYNJ37304F NON-VASCULAR PACK DYNJ56386B OR HYBRID-MRMC DYNJ907758 PACER PACK DYNJ40952 PAIN PACK DYNJ60715 PICC PHC DYNJ37484B ROBOTIC PACK DYNJ908706A THORACOTOMY PACK-LF DYNJ0101339J DYNJ69090 VENOUS PACK DYNJ56260B
Reason for recall
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
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-2585-2026. 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.