Skip to main content
Recall Canary
Medline Convenience Kits with BD ChloraPrep Clear 1mL Applicators
← Back to all recalls
MEDICAL DEVICE RECALLMODERATE

Medline Convenience Kits with BD ChloraPrep Clear 1mL Applicators

Medline recalls Convenience Kits with BD ChloraPrep Clear 1mL Applicators over possible open or incomplete seals.

What to do

Check your kit for the affected BD ChloraPrep Clear 1mL Applicators. Stop using the applicators and contact Medline or your healthcare provider for instructions on returning the product and obtaining a replacement.

Recalled
Listed
Updated
Agency
FDA
Firm
Medline Industries, LP
Recall ID
99561
Status
ONGOING

Recall at a glance

Quantity recalled
222,653 total

Why it was recalled

Medline is recalling Convenience Kits containing BD ChloraPrep Clear 1mL Applicators due to a downstream recall of the applicators. The affected applicators may have an open or incomplete seal on their packaging, which could lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

Is mine affected?

This recall covers 13 products. Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators

ProductLot codeUDI-DI
PAIN PRE OP KIT DYKS1476A25IBJ918, 25KBN677, 25LBU066, 26BBD77510198459362835
C-SECTION PREP DYNJ32702B25BBB005, 25GBY063, 25KBI862, 25LBT688, 26CBG21110193489431070
BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 DRAWER #4 ACC010479A DRAWER 2 ACC010690 ACC010875 DRAWER 3 SYR/DRS/MON/NG 1 OF 3 ACC011073 DRAWER 4 CIRCULATION ACC011088 DRAWER 5 - LEFT BOX ACC011067 LABOR TRIAGE KIT - LF #13232 DYKM1564 DYKM1564A LINEN UNIVERSAL PACK DYNJT10325 MAC KIT DYKS1089B NICU LINE PACK DYNJ63410 PEDIATRIC BLOOD CULTURE KIT DYNDH1363 RRMC CODE CART DRAWER 3 ACC010770 STANFORD TIME TO POSITIVITY DYNDH1591 STUDENT PRACTICE BAG W LOGO EDUC1043 EDUC1043A SUTURED SHEATH W/SCI #113198 DYKM1496 IV START KIT DYNDV252024JMB689, ACC010972, 25DDA151, 25DDA401, 25EDA655, ACC010479A, 25BDB620, ACC010690, 24LDB023, 25BDA230, 25GDA245, 25JDB903, 25KDB182, 25LDA088, 25LDA809, 26ADC073, 26CDA991, 26DDB182, 26EDA950, 26EDB485, 26FDB456, ACC010875, 24JDA648, 25CDB776, 25JDB205, 25KDB028, 25LDB271, 26DDA182, 26DDA786, 26EDA629, ACC011073, 25LDA072, ACC011088, 26BDA548, 26GDA090, ACC011067, 25KDA639, 25LDA980, 26CDB158, DYKM1564 (+82 more, see the official notice)10888277860209, 10198459303289, 10195327131517, 10195327433307, 10198459113659, 10198459569333, 10198459589577, 10198459529184, 10889942754571, 10198459805165, 10198459787324, 10193489306286, 10193489737431, 10888277795464, 10195327576998, 10193489497236, 10195327425531, 10198459334559, 10889942636082, 10653160384045
ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE DYNDH1866 BLOOD CULTURE KIT DYNDH1462B DYNDH1622C DYNDH1622D DYNDH1622F DYNDH1715B DYNDH2028 DYNDH2048 BLOOD CULTURE-NB DYNDH2089 BLOOD DRAW KIT DYLAB1081 FLOORS BLOOD DRAW KIT DYLAB1080 PEDS BLOOD CULTURE KIT DYNDH1445C PERIPHERAL BLOOD CULTURE KIT DYNDH2350 WICHITA BLOOD CULTURE COLLECT DYNDH209324IBK133, 24KBE072, 24LBD419, 25GBT189, 25IME347, 25IMI389, 25KMA880, 25KME693, 26BMH685, 26CMH411, 26DME199, 26EMB070, 26EMF542, 26FMC275, DYNDH1866, 24HBW237, 24IBI505, 24JBI308, 24KBH534, 24LBI545, 25ABC487, 25ABO282, DYNDH1462B, 24HBV192, 24IBE469, 24IBV947, 24JBA557, 24JBI310, 24KBJ830, 24KBJ831, 24KBN934, 24LBN283, 24LBP258, DYNDH1622C, 24IBE381, 24IBL908, 24JBF575, 24JBS022, 24KBN937, 24LBI552 (+73 more, see the official notice)10195327502492, 10195327400958, 10195327662462, 10195327509873, 10198459234965, 10198459658884, 10195327407094, 10198459035715, 10198459106125, 10198459244070, 10198459199608, 10198459199615, 10195327502614, 10198459779251, 10198459256967
BLOOD CULTURE KIT 2 W/CONNECT DYNDH1487A25AMD225, 25BMA495, 25GMD834, 25HMJ685, 26AMD781, 26DMI370, 26FMG952, 26FMJ73910193489484311
PATIENT ADMIN KIT DYKA1384B DYKA1384C WELCOME KIT DYKS1206D25GBS617, DYKA1384C, 25IBF898, DYKS1206D, 25HBI181, 25JBJ452, 25LBJ223, 26ABT372, 26CBF527, 26EBH73310198459415753, 10198459485206, 10198459414794
BASIN PACK-LF DYNJ42828B EYE BASIN TRAY-LF DYNJ42832B25GBQ173, 25HBB240, 25JBD028, 25LBL133, 26ABU673, 26CBN583, 26EBD855, 26FBO892, 25LBE548, 26BBG040, 26CBH272, 26EBC041, 26FBD49710198459425516, 10198459425530
LABOR CDS CDS981762B VAG DELIVERY ADMISSION BAG DYKA1054F24JBE456, 24JBN932, 24KBJ154, 25ABK513, 25CBL684, 25HBK086, 25IBM188, 25KBL720, 25LBF812, 25LBU497, 26ABM665, 26CBH544, 26CBT272, 26FBK806, DYKA1054F, 24ILA823, 24JLA285, 24LLA226, 24LLB033, 25BLA842, 25ELA624, 25GLA270, 25HLB055, 25KLA019, 25KLA187, 26BLA150, 26CLA717, 26DLA410, 26ELA772, 26FLA75610193489306767, 10193489312607
Show all 13 products
ProductLot codeUDI-DI
CATARACT PREOP KIT DYKS1583A24KBP38810198459146640
OPEN HEART CDS983348AA CDS983348AB24IBK346, 24JBK539, 25CBF097, 25HBB232, 25HBB761, 25HBH209, 25HBU907, 25JBQ17610195327385088, 10198459136986
IV START KIT LAB DRAW-SH CDS860014Q IV START KIT DYKM1000B IV START KIT LAB DRAW-SH CDS860014P ULTRASOUND GUIDED PIV START KI DYNDV268426ABR359, 26BBP789, 26CBL940, 26DBK987, 26FBK255, 26FBK816, DYKM1000B, 24KMD782, 24LMH404, 25AMD765, 25BMD744, CDS860014P, 24IBA155, 24JBY045, 24LBM014, 25HBR509, 25JBX951, DYNDV2684, 24LBP24310198459629822, 10889942508143, 10888277797819, 10198459185465
DELUXE PRE OP KIT DYKS2018 GENERAL PREOP KIT DYKS1584A PRE OP KIT DYKS1216I PRE-OP KIT DYKM1398B25GMI043, DYKS1584A, 24JBA740, 25ABF244, DYKS1216I, 25GBP888, 25JBD789, 26ABL474, 26CBF334, 26DBD640, 26EBB855, 26FBC632, DYKM1398B, 25HBI183, 25JBK222, 25KBA990, 25LBJ990, 26BBI525, 26CBJ249, 26EBQ630, 26FMF18910198459188480, 10198459146633, 10198459362668, 10198459413827
ORTHO ASPIRATION KIT DYKM1636A26EBI94010889942925858

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other Contamination recalls

Other recent recalls from Medline Industries, LP

All recalls from Medline Industries, LP

← Back to all recalls

Editorial summary by Recall Canary · summary updated 2026-09-01 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification