Reported Sep 2, 2026 · Ongoing · Updated Sep 7, 2026

Medline medical convenience kits, labeled as

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?

56 of 56 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ0966146F1019348991637940193489916370Medline Kit , UDI/DI 10193489916379 (each) 40193489916370 (case), Lot Number 23HBC070
DYNJ40154D1088994296873240889942968733Medline Kit , UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 24CBA416
DYNJ40154D1088994296873240889942968733Medline Kit , UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23CBS214
DYNJ40154D1088994296873240889942968733Medline Kit , UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23FBC803
DYNJ40154D1088994296873240889942968733Medline Kit , UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23GBU042
DYNJ40154D1088994296873240889942968733Medline Kit , UDI/DI 10889942968732 (each) 40889942968733 (case), Lot Number 23IBO417
DYNJ40154F1019532767929340195327679294Medline Kit , UDI/DI 10195327679293 (each) 40195327679294 (case), Lot Number 24EBH594
DYNJ40154F1019532767929340195327679294Medline Kit , UDI/DI 10195327679293 (each) 40195327679294 (case), Lot Number 24FBQ494
DYNJ40154F1019532767929340195327679294Medline Kit , UDI/DI 10195327679293 (each) 40195327679294 (case), Lot Number 24JBK316
DYNJ44480D1019845924172740198459241728Medline Kit , UDI/DI 10198459241727 (each) 40198459241728 (case), Lot Number 25CDA135
DYNJ58928A1019348976397340193489763974Medline Kit , UDI/DI 10193489763973 (each) 40193489763974 (case), Lot Number 23HBK833
DYNJ832961019532725891740195327258918Medline Kit , UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 24FBQ476
DYNJ832961019532725891740195327258918Medline Kit , UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 23EBI941
DYNJ832961019532725891740195327258918Medline Kit , UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 23HBX888
DYNJ832961019532725891740195327258918Medline Kit , UDI/DI 10195327258917 (each) 40195327258918 (case), Lot Number 22KBR883
DYNJ890061019845924197040198459241971Medline Kit , UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25JMC017
DYNJ890061019845924197040198459241971Medline Kit , UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25KMB183
DYNJ890061019845924197040198459241971Medline Kit , UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25AMG343
DYNJ890061019845924197040198459241971Medline Kit , UDI/DI 10198459241970 (each) 40198459241971 (case), Lot Number 25DMJ252
DYNJ900537D1088827777520640888277775207Medline Kit , UDI/DI 10888277775206 (each) 40888277775207 (case), Lot Number 23ABM594
Amount recalled
2262 kits

This recall covers 19 products

The agency filed one notice per product. You are reading one of them; the other 18 are below.

6 more are in the archive.

Where it was sold

Why it was recalled

Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 3:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.