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?

49 of 49 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS985246J1019348923239440193489232395Medline Kit , UDI/DI 10193489232394 (each) 40193489232395 (case), Lot Number 22HMB295
CDS985246J1019348923239440193489232395Medline Kit , UDI/DI 10193489232394 (each) 40193489232395 (case), Lot Number 22IMB860
DYNJ32770V1019532709011140195327090112Medline Kit , UDI/DI 10195327090111 (each) 40195327090112 (case), Lot Number 22FMB806
DYNJ40095D1019532728125040195327281251Medline Kit , UDI/DI 10195327281250 (each) 40195327281251 (case), Lot Number 23GMI744
DYNJ42844D1019348988056440193489880565Medline Kit , UDI/DI 10193489880564 (each) 40193489880565 (case), Lot Number 25EBV362
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 25CMH980
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 25FMB096
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 25GMA066
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 25GMH940
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 25BMI081
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 25IMC735
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24DME519
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24EMG256
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24GMJ491
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24IMA243
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24JMA162
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24JMD784
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24KMI470
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24ABN077
DYNJ45121I1019348988763140193489887632Medline Kit , UDI/DI 10193489887631 (each) 40193489887632 (case), Lot Number 24ABN475
Amount recalled
3468 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.