Reported Apr 29, 2026 · Ongoing
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes JUDKINS PACK DYNJ51126 ANGIO…
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
10 of 10 products
| Model / number | Product as published |
|---|---|
DYNJ32555C | Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes JUDKINS PACK DYNJ51126 ANGIO PACK |
DYNJ46153B | TRAY |
DYNJ26855F | PACK |
DYNJ24530I | PACK-M-LF |
DYNJ0220880V | TRAY-LF |
DYNJ0545064X | LAB ANGIO PACK-LF |
DYNJ39057C | LAB PACK |
DYNJ61015B | ANGIOGRAPY SET UP |
DYNJ47710C | PACK |
PHS677784013A | ANGIO PACK-LF |
- Lot codes and dates
- DYNJ51126 UDI-DI 10889942122820 (EA) 40889942122821 (CS) LOT 20ADA585 DYNJ32555C UDI-DI 10193489859485 (EA) 40193489859486 (CS) LOTSUDI-DI 10193489368321 (EA) 40193489368322 (CS) LOTS 22BBB494 22BBB497 DYNJ46153B UDI-DI 10193489853643 (EA) 40193489853644 (CS) LOTS
21HMF69921IMF81321JMA85521KMD60522DMB42322FMD57422HMB60822LMA16923BMA11423EMB81723EMG15323KMB69223KMH35923LMH08524AMC56324CMD58724DMD25624DMG30524FMD71724IMI65024JMC830DYNJ66631
UDI-DI 10888277012042 (EA) 40888277012043 (CS) LOTS23EBM22523FBC88423HBP27823IBV99923KBC31923LBK12524CBF10024DBE95224FBP26224GBN96024HBO92124IBO00724IBU94124JBK66924LBK644DYNJ26855F
UDI- DI 10193489674910 (EA) 40193489674911 (CS) LOT 24ABU775 DYNJ0220880V UDI-DI 10889942054688 (EA) 40889942054689 (CS) LOTS20CBI04920EBB60020FBK90020GBD33120GBL79520IBC78820JBM78620KBF14821BBK24421EBR32721HBB84921IBQ80921OBA396DYNJ24530I
UDI-DI 10889942138630 (EA) 40889942138631 (CS) LOTS23HLA50523HLB25723JLA02123JLA05923KLA12123KLA23123KLA58223LLA81724ELA40524ELA79624HLA59625AMI60925BMH66025CMA79725DMF893DYNJ30077D
UDI-DI 10193489747621 (EA) 40193489747622 (CS) LOTS23FBQ47923LBL70724CBC49524EBQ34624GBK89524HBD02324HBP29024JBJ112DYNJ0545064X
UDI-DI 10193489765519 (EA) 40193489765510 (CS) LOT 24BBD166 DYNJ61015B UDI-DI 10193489368888 (EA) 40193489368889 (CS) LOTS 23CMG023 23FBN151 DYNJ47710C UDI-DI 10889942214495 (EA) 40889942214496 (CS) LOTS20BBL11520CBA64920DBB93320DBP59520HBW93920KBI81521ABK03921ABK542DYNJ39057C
UDI-DI 10193489604337 (EA) 40193489604338 (CS) LOTS23FBF10923GBB67723JBP27023LBO68824DBD35624FBP32624IBC34024KBJ788PHS677784013A
***Updated 5/20/26 - The following lots were included in the customer notification but not in the FDA submission.*** DYNJ0220880V Lots20BBR30120IMA68321BMC46721CMC05221FMD14021IMF22922AMA95922AME45823GMA49123GMD585
25LMA384; DYNJ30077D Lots21DLA45321FLA08321ILA14721KLA05922ALA84922DLA70722FLA70022HLA27222ILA18822ILA23722ILA64122JLA66222KLA83622KLA93922LLA39925KMB595
24CBR583; DYNJ32555C Lots21ABB34821ABR32721DBQ39721FBM87321GBL53921IBB39021JBO22021KBC30221KBV07921LBT52822ABZ83422DBD74422EBG37522JBK53322KBO29122OBM41123ABD82423ABO41923DBB78823EBS95123HBB56323IBG76223JBT149
25BMD349; DYNJ46153B Lots21DMA30121DMD92921EMB68621FMA16322KMD64423AMB07324LMH11425BMA103
25EBA187; DYNJ47710C Lots21CBL35921FBE61821GBF34621HBQ71621IBW15421KBI85321LBA40122ABE87722BBW97822CBU32322EBN72522FBQ42022GBJ22922HBD58122IBL25822JBM06122KBD44022NBA19923ABG76923BBE72425BBR850
25CBJ501; DYNJ61015B Lots21CBM12021GBL62221KBA84921KBA92522ABX23922CBP65422JBI02322LBR93323BBT61125BBF414
23DMC707; DYNJ66631 Lots 21IBH359 21VBC892 22BBW852 22DBJ281 22EBJ532 22GBA38021AMB13121BMB92321BMC12821CMD38421DMD44121FMD10221GME20521JMG65222AMD05022AME24422DME86922FMA87222FMD24622GMG53422IMB77922IMF57422JMG96323AMD81523BMB886
- DYNJ51126 UDI-DI 10889942122820 (EA) 40889942122821 (CS) LOT 20ADA585 DYNJ32555C UDI-DI 10193489859485 (EA) 40193489859486 (CS) LOTS
- Amount recalled
- 270,311 total
This recall covers 39 products
The agency filed one notice per product. You are reading one of them; the other 38 are below.
26 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Unapproved design changes to the products outside of the 510(k) clearance.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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