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RecallWatchMedical Device Safety
Class IIOngoingZ-3070-2026

Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULT…

Medline Industries, LPNorthfield, IL, United StatesReported Sep 9, 2026 · 6 days ago
Legal News Analyst ·

Reason for recall

Downstream recall - manufacturer recalled specific lots of BD ChloraPrep Clear - 1mL Applicators. Affected product may exhibit an open or incomplete seal on the packaging of the applicator. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators 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 KITDYNDV2520
    UDI-DI 10888277860209
    141 affected lots
    24JMB689ACC0109721019845930328925DDA15125DDA40125EDA655ACC010479A10195327131517
    +133 more25BDB620ACC0106901019532743330724LDB02325BDA23025GDA24525JDB90325KDB18225LDA08825LDA80926ADC07326CDA99126DDB18226EDA95026EDB48526FDB456ACC0108751019845911365924JDA64825CDB77625JDB20525KDB02825LDB27126DDA18226DDA78626EDA629ACC0110731019845956933325LDA072ACC0110881019845958957726BDA54826GDA090ACC0110671019845952918425KDA63925LDA98026CDB158DYKM15641088994275457124HBW93724JBX63424LBR08525GBH20925IBK59025LBD52526ABI52426BBM58526DBC555DYKM1564A1019845980516526FBK649DYNJT103251019845978732426EBM25026FBA47026FBF05526FBH55326FBH554DYKS1089B1019348930628624JMG84624LMD91825GMD75925GMK43125IMF05025KMJ02626BMC07326DMI048DYNJ634101019348973743124LDB85125BDA890DYNDH13631088827779546424IBH34924IBS20024JBQ16024KBN44724LBG38024LBI54725ABW56325DBH95425GBD82425HBT17225IBO19225JBB92125JBQ987ACC0107701019532757699825HDA87825IDA08725IDA81725JDB31725KDB34025LDB06126ADA01226ADA15926ADB38026ADC07226BDA63326CDA678DYNDH15911019348949723624JMA96625GMD75225LMJ15426AME49726BMA25226DMI08826EMH91426FMH45326FMK588EDUC10431019532742553124KDA25824KDA88024KDA963EDUC1043A1019845933455925FLA81725GLA09025KLA07725KLA69326CLB16526CLB165Z26ELA472DYKM14961088994263608224KBL243DYNDV2520106531603840452024111990

What the firm is doing

Firm began notifying consignees on 7/20/2026 via First-Class Mail and email. Medline Industries LP instructed customers to request stickers to over-label the affected convenience kits with a label indicating to remove the affected component and replace it with product from supply. No kits are to be returned.

DistributionShow details

US Nationwide distribution.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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