Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026
Medline Convenience Kits
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?
Medline Convenience Kits
5 of 5 products
| Model / number | Product as published |
|---|---|
DYNJT8784 | MFC CRANIOTOMY PACK |
DYNJ0369348Q | SLUH CRANIOTOMY PACK-LF |
DYNJ0369348R | SLUH CRANIOTOMY PACK-LF |
DYNJ0369348S | SLUH CRANIOTOMY PACK-LF |
DYNJ0369348T | SLUH CRANIOTOMY PACK-LF |
- Lot codes and dates
13 of 13 products
Products covered by this recall # Barcodes Product as published 1 1019845920063240198459200633Lot Number: 26EBN238; 2) DYNJ0369348Q, UDI-DI: 10198459200632(each), 40198459200633(case) 2 1019845920063240198459200633Lot Number: 25GBC553; 3) DYNJ0369348Q, UDI-DI: 10198459200632(each), 40198459200633(case) 3 1019845920063240198459200633Lot Number: 25FBA082; 4) DYNJ0369348Q, UDI-DI: 10198459200632(each), 40198459200633(case) 4 1019845920063240198459200633Lot Number: 25EBP462; 5) DYNJ0369348Q, UDI-DI: 10198459200632(each), 40198459200633(case) 5 1019845920063240198459200633Lot Number: 25DBU966; 6) DYNJ0369348Q, UDI-DI: 10198459200632(each), 40198459200633(case) 6 1019845944209440198459442095Lot Number: 25CBS315; 7) DYNJ0369348R, UDI-DI: 10198459442094(each), 40198459442095(case) 7 1019845944209440198459442095Lot Number: 25JBB880; 8) DYNJ0369348R, UDI-DI: 10198459442094(each), 40198459442095(case) 8 1019845965631640198459656317Lot Number: 25HBF280; 9) DYNJ0369348S, UDI-DI: 10198459656316(each), 40198459656317(case) 9 1019845965631640198459656317Lot Number: 26CBK932; 10) DYNJ0369348S, UDI-DI: 10198459656316(each), 40198459656317(case) 10 1019845965631640198459656317Lot Number: 26BBT826; 11) DYNJ0369348S, UDI-DI: 10198459656316(each), 40198459656317(case) 11 1019845973382640198459733827Lot Number: 26BBT935; 12) DYNJ0369348T, UDI-DI: 10198459733826(each), 40198459733827(case) 12 1019845973382640198459733827Lot Number: 26EBG096; 13) DYNJ0369348T, UDI-DI: 10198459733826(each), 40198459733827(case) 13 Lot Number: 26DBM677 - Amount recalled
- 486 kits
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.
This product could cause temporary or reversible health problems — stop using it.
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