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RecallWatchMedical Device Safety
Class IIOngoingZ-3073-2026

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

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 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 COLLECTDYNDH2093
    UDI-DI 10195327502492
    127 affected lots
    24IBK13324KBE07224LBD41925GBT18925IME34725IMI38925KMA88025KME693
    +119 more26BMH68526CMH41126DME19926EMB07026EMF54226FMC275DYNDH18661019532740095824HBW23724IBI50524JBI30824KBH53424LBI54525ABC48725ABO282DYNDH1462B1019532766246224HBV19224IBE46924IBV94724JBA55724JBI31024KBJ83024KBJ83124KBN93424LBN28324LBP258DYNDH1622C1019532750987324IBE38124IBL90824JBF57524JBS02224KBN93724LBI552DYNDH1622D1019845923496525GBA90525GBI39825GBT18225HBN20325IBH34525IBQ48625IBS19225JBN62925KBK71825LBI568DYNDH1622F1019845965888426BBL47726CBA40726CBD37626DBA85526DBL28626FBF458DYNDH1715B1019532740709424IMF148DYNDH20281019845903571524KBL250DYNDH20481019845910612524JBK98725GBI40125GBT18325IBB66625JBC74225KBD09325KBK72325LBI56725LBO86326ABL65326CBO16526DBB15326DBE99426EBF75226FBN334DYNDH20891019845924407025KMJ96726BMI73126FMF126DYLAB10811019845919960824LMH50625HMA38625HMD68525IMF41525JMB43825JMC50326AML13826BMJ27726EMB352DYLAB10801019845919961524LMG08525AMH560DYNDH1445C1019532750261424IBK13124KBB55124LBU13925GBQ02325GBU01625HMI51525IMB46525IME35025JMI24726CMB60926DMH68626FMC27426FMC274DDYNDH23501019845977925126FBM766DYNDH20931019845925696726ABP408

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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