Reported May 6, 2026 · Ongoing
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows
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?
53 of 53 products
| Model / number | Barcodes | Product as published |
|---|---|---|
DYNJ40566C | 40889942469650 | Medline Kit Number/ : UDI/DI each10889942469659, UDI/DI case 40889942469650, Lot Number: 22BBJ540 |
DYNJ40566C | 40889942469650 | Medline Kit Number/ : UDI/DI each10889942469659, UDI/DI case 40889942469650, Lot Number: 21LBM539 |
DYNJ40566C | 40889942469650 | Medline Kit Number/ : UDI/DI each10889942469659, UDI/DI case 40889942469650, Lot Number: 21IBX286 |
DYNJ40566C | 40889942469650 | Medline Kit Number/ : UDI/DI each10889942469659, UDI/DI case 40889942469650, Lot Number: 21HBM832 |
DYNJ47491F | 40193489586726 | Medline Kit Number/ : UDI/DI each10193489586725, UDI/DI case 40193489586726, Lot Number: 21KMD114 |
DYNJ58274 | 40889942840725 | Medline Kit Number/ : UDI/DI each10889942840724, UDI/DI case 40889942840725, Lot Number: 22FMI371 |
DYNJ58274 | 40889942840725 | Medline Kit Number/ : UDI/DI each10889942840724, UDI/DI case 40889942840725, Lot Number: 21IMD775 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 23JBD782 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 23HBY508 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 23GBQ615 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 23EBR984 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 23EBD017 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 23BBO048 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 22JBI096 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 22FBA057 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 22CBA050 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 21IBG464 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 21GBJ471 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 21EBA373 |
DYNJ58344 | 40889942841722 | Medline Kit Number/ : UDI/DI each10889942841721, UDI/DI case 40889942841722, Lot Number: 21DBG514 |
- Amount recalled
- 7004 kits
This recall covers 38 products
The agency filed one notice per product. You are reading one of them; the other 37 are below.
25 more are in the archive.
Why it was recalled
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
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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