Medline Convenience Kits containing select SKUs of 10mL Polycarbonate… — Class II medical device recall Z-1890-2026

Ongoing recall by Medline Industries, LP, reported 2026-04-29, distributed nationwide. Unapproved design changes to the products outside of the 510(k) clearance.

Recall number	`Z-1890-2026`
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	2026-04-17
Reported by FDA	2026-04-29
Distributed	Nationwide (US)
Countries outside the US	BB, CA, PA
Quantity	270,311 total
Reason classes	unapproved product
UPC / GTIN / UDI-DI	`10195327542320`, `10195327571252`, `10195327576530`, `10195327586508`, `10195327591298`, `10195327593346`, `10195327600006`, `10195327617547`, `10195327624002`, `10195327657901`, `10195327666323`, `10195327675813`, `10195327686222`, `10195327686499`, `10198459004124`, `10198459014956`, `10198459018800`, `10198459021541`, `10198459022395`, `10198459026263`, `10198459053115`, `10198459053184`, `10198459072499`, `10198459077760`, `10198459099755` and 61 more
Lot numbers	`23LBI856`, `23LBS736`, `24ABA334`, `24ABS351`, `24ADC205`, `24BMC933`, `24BMG223`, `24BMJ645`, `24CBJ902`, `24CLA801`, `24CMA913`, `24CMG670`, `24DDA061`, `24DLA314`, `24DMA039`, `24DMC608`, `24DMF381`, `24DMG180`, `24DMG627`, `24EBG787`, `24EBI547`, `24EBQ265`, `24EBQ331`, `24ELA254`, `24EMH743`, `24EMH999`, `24FBG624`, `24FBI743`, `24FBM384`, `24FBO911`, `24FBR560`, `24FBR752`, `24FDA217`, `24FLA167`, `24FLA499`, `24FME392`, `24FMI037`, `24GBA517`, `24GBE275`, `24GBE276` and 207 more
Model numbers	`DYNJ21259O`, `DYNJ30551J`, `DYNJ51423G`, `DYNJ61373B`

Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADD A ENDOVASCULAR PACK-LF DYNJ0429339L, DYNJ0429339M ANGIO ARTERIOGRAM PACK-LF DYNJ0774026K ANGIO KIT PACK DYNJ83746B ANGIO TRAY NO LIDO DYNJ85557A ANGIOGRAPHY PACK II DYNJ17218S, DYNJ17218T ARTERIOGRAM NEURO PACK-LF DYNJ0842499L ARTERIOGRAM PACK-LF DYNJ0842478M CARDIAC CATH II PK DYNJ21259O CARDIAC CATH PACK DYNJ68653D CATH LAB ANGIOGRAPHY PACK DYNJ50779G CATH LAB-LF DYNJ51423G CRANIOTOMY PACK-LF DYNJ0101292I DEEP BRAIN STIMULATION PACK DYNJ0842793I ENDO VASCULAR MINOR DYNJ87263 GENERAL ENDO PACK-LF DYNJ0842873L LEFT HEART DYNJ45984J LIPO PACK DYNJ87218 MAA Y90 TRAY DYNJ82191D MAIN OR CATH LAB DYNJ61373B MINIMALLY INVASIVE PACK-LF DYNJ0843063M NEURO CERVICAL PACK DYNJ0101287M NEURO RADIOLOGY RICHMOND DYNJ68365F NEURO VP SHUNT PACK-LF DYNJ0843121L NON-VASCULAR PACK DYNJ56386C, DYNJ56386D OR ANGIOGRAM PACK-LF DYNJ83656A, DYNJ83656B OR RADIOLOGY PACK DYNJ62747A PERCUTANEOUS ARTERIAL CATH PK DYNJ30551J PERIPHERAL ARTERIOGRAM RAD DYNJ61383C PICC ABSCESS PACK-LF DYNJ0774005I PICC TRAY DYNJ30554I PODIATRY PACK DYNJ46333G POSTERIOR SPINE PACK-LF DYNJ0843339P RRMC ANGIO PACK DYNJ36338D SPECIAL PROCEDURE PACK DYNJ88258 VASCULAR ACCESS PACK-LF DYNJ0101291G VASCULAR HYBRID DYNJ57543K VASCULAR PACK DYNJ82220D VISCERAL ANGIOGRAM PACK-LF DYNJ0429121M WPH EP PACK DYNJ62745A

Reason for recall

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

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-1890-2026. 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.