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?

29 of 29 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJT65481019845955876440198459558765Medline Kit , UDI/DI 10198459558764 (each) 40198459558765 (case), Lot Number 25JMF561
DYNJ44504G1019845924195640198459241957Medline Kit , UDI/DI 10198459241956 (each) 40198459241957 (case), Lot Number 25EDA305
DYNJ44504G1019845924195640198459241957Medline Kit , UDI/DI 10198459241956 (each) 40198459241957 (case), Lot Number 25EDB254
DYNJ45419F1019532762568940195327625680Medline Kit , UDI/DI 10195327625689 (each) 40195327625680 (case), Lot Number 24JMF418
DYNJ45419F1019532762568940195327625680Medline Kit , UDI/DI 10195327625689 (each) 40195327625680 (case), Lot Number 24JMJ129
DYNJ46024F1019532723701140195327237012Medline Kit , UDI/DI 10195327237011 (each) 40195327237012 (case), Lot Number 23HBJ773
DYNJ54479C1019348946025440193489460255Medline Kit , UDI/DI 10193489460254 (each) 40193489460255 (case), Lot Number 23HBA720
DYNJ58006B1019348986738140193489867382Medline Kit , UDI/DI 10193489867381 (each) 40193489867382 (case), Lot Number 23BMC930
DYNJ58006B1019348986738140193489867382Medline Kit , UDI/DI 10193489867381 (each) 40193489867382 (case), Lot Number 23FMD505
DYNJ58006B1019348986738140193489867382Medline Kit , UDI/DI 10193489867381 (each) 40193489867382 (case), Lot Number 23JMH313
DYNJ58006B1019348986738140193489867382Medline Kit , UDI/DI 10193489867381 (each) 40193489867382 (case), Lot Number 23LME066
DYNJ58006B1019348986738140193489867382Medline Kit , UDI/DI 10193489867381 (each) 40193489867382 (case), Lot Number 22CMG565
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 24BME326
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 24EMF925
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 23AMJ184
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 23EMD739
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 23IME138
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 23KMB648
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 23LMB107
DYNJ58014A1019348986400740193489864008Medline Kit , UDI/DI 10193489864007 (each) 40193489864008 (case), Lot Number 23LMH426
Amount recalled
974 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.

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By hazard

Other recalls from Medline Industries, LP

36 in total.

Where it was distributed

All recall categories · Browse the whole archive

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.