Reported Apr 29, 2026 · Ongoing
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B 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?
- 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
- Lot codes and dates
- DYNJ50783B UDI-DI 10193489227376 (EA) 40193489227377 (CS) LOT 23FBF183 DYNJ37485C UDI-DI 10193489760002 (EA) 40193489760003 (CS) LOTSUDI-DI 10193489789164 (EA) 40193489789165 (CS) LOT 23HMI416 DYNJ39931D UDI-DI 10193489459364 (EA) 40193489459365 (CS) LOTS
20BBX69220DBC08920EBG81620FBR15320HBN28820IBK57820KBW29121BBB26621CBW19821FBH67421GBS84021GBS84221JBU70321LBX72122BBV33722EBN70822IBJ46722JBH99622KBU90122OBJ15023ABG61523BBF60323CBC306DYNJ53064B
UDI-DI 10889942825103 (EA) 40889942825104 (CS) LOTS 23FMA240 24EBR693 24GLB224 24HLA705 24JLA904 NAM0003 UDI-DI 10193489222555 (EA) 40193489222556 (CS) LOTS23BBB18223DBK36324HBJ42724JBI91524JBV98524KBH81725GBI67025IBS445DYNJ0948060F
UDI-DI 10195327507923 (EA) 40195327507924 (CS) LOT 24FMC929 DYNJ59903B UDI-DI 10195327131203 (EA) 40195327131204 (CS) LOTS20DBO37520GBC31720GBJ71920HBC15920HBD81520HBF51920IBA51423CMC98123DMC49023DMF16123GMA35323HME05723HMG26423IMF17323JMF87823JMH82923KME88523LMA78023LMD08823LMG05924AMF16724AMH12824EMG74724HMJ04124JMC680DYNJ61542D
UDI-DI 10195327481506 (EA) 40195327481507 (CS) LOTS 23LBN462 24ABC179 DYNJ44027F UDI-DI 10193489783490 (EA) 40193489783491 (CS) LOTS23EBQ21623HBC08923IBE17623KBL43923LBO49424ABL93824CBQ70824EBB10824FBA58424FBN89724JBC98324JBO34924KBB06124KBT24224LBP491DYNJ84872A
UDI-DI 10193489631784 (EA) 40193489631785 (CS) LOTS 23ELA677 23GLA263 23KLB156 ***Updated 5/20/26 - The following lots were included in the customer letter but not the FDA submission.*** DYNJ0948060F lots21FLA18421FLA91021ILA78321JLA54221LLA17722ALA73122BLA80222DLA49722ELA81822FLA43222GLB16122HLB06222JBC79522JBM04522KBO20922KBO21023DBR51223FBQ56323GBK95523HBY70723JBT73823KBF31123KBU56324ABW46724GBK56024HBB84324IBI79824IBR64324JBF292DYNJ62176
25ELA692; DYNJ39931D lots21AMA91921AMB49121BMC17821HMF80021JMG47222AMB40622CMI92722EMC82422GMF26122IMA65122JMG95222KME54922LMD53123AMD74523AMJ62623CMB80823DMC06023EMB61323EMG67223GMG69323GMI43823IMG05523KBR80224ABP56725ALA62225ALA67825CLA31725DLA949
24GBO821; DYNJ44027F lots 21BLA158 21CLA034 21DLA700 25EBE984 25EBU842; DYNJ50783B lots21ABW86121CBY11821DBN14021HBN10521KBO17121LBP80821LBP81122CBY15422FBA26322JBU79923BBR77723BBT17723EBS91823FBO98323GBR31523GBW41023HBJ97623IBJ86323KBC96223LBU94424ABK32324ABP44224BBH773
23EBC283; DYNJ59903B lots21DBL97221FBK45221GBA22721IBA35421JBO23921KBP32721LBB84521LBU42522DBC32222DBN51722EBK09022FBK17222HBU11422KBQ55122KBQ55223BBJ72523CBO941
25DBF626; DYNJ62176 lots22EBI49922FBF02822FBR42522IBJ53822LBQ31123ABN46623CBJ59623CBP099
24JLA075; DYNJ84872A lots 23IBS046; NAM0003 lots21ALA43721BLA17821BLA23821BLA35221CLA51621GLB10022ALA16322BLB20722ELB04122KLA09222LLA72823ALA74323BLA18423KLB12424BLA18024ELA039
21BBF21821CBE23021DBV01821EBS50821GBI65321KBO48621LBB47022CME11022EMH49625AMG21225BMA48125BMF35725BMH68425DMH01425DMH50325EMD61725EMI879
- DYNJ50783B UDI-DI 10193489227376 (EA) 40193489227377 (CS) LOT 23FBF183 DYNJ37485C UDI-DI 10193489760002 (EA) 40193489760003 (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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