Medline Convenience Kits
The kits contain neurological sponges with potential for unexpected variability of endotoxin levels.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Medline Industries, LP, of Northfield, Illinois, recalled Medline Convenience Kits containing 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. The company began the recall on August 10, 2026, and the kits were distributed nationwide.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Match the list below, then check the codes the FDA notice also names.
Medline Convenience Kits
- UDI-DI
- 10198459778865
- 40198459778866
- 10193489801170
- 40193489801171
- 10195327025892
- 40195327025893
- 10195327295417
- 40195327295418
- Lot
- 26GBA998
- 23HLA649
- 23GLA935
- 23GLA081
- 23CLA457
- 23BLA516
- 22IBO169
- 22GBD964
- 22DBU156
- 24KBH955
- 24JBB595
- 24GMF624
- 24CMJ263
- 24BMK244
- 24AMF230
- 23JBJ151
- 23FBG216
- 23EBC638
- 23CBI768
- 23ABM980
- 23ABI593
- 23HMB096
- 23HMC253
- 23HBJ773
- 23HMC669
- 23HMA338
- 23HBD216
- 23CBG270
- 23BBB578
- 22LBP140
- 23HBA720
- 23HBP930
- 23GBT243
- 23HLA933
- 23GBS430
- 23HBG744
- 23GBR467
- 23HMA427
- 26CMI592
- 22IBC626
- 22HBS240
- 24JMH504
- 24JMD199
- 24IMG055
- 24GMJ361
- 24EMD234
- 24DMG428
- 24BMI349
- 24AMG705
- 23LMF389
- 23JMK268
- 23JMB370
- 23IMC078
- 23HMH387
- 23GMD961
- 23DME252
- 23DMB260
- 23CMG273
- 26GMG394
- 26FMD545
- 26DMD616
- 26DMA441
- 26DMA421
- 25KMJ807
- 25KMB625
- 25HMI954
- 25FMC018
- 25EMF909
- 25CMF056
- 25AMF815
- 25GBW221
- 25GBD210
- 25EBM992
- 25DBN524
- 25BBQ529
- 24LBP184
- 24KBH441
- 24JBD802
- 24IBK611
- 24DBV145
- 24CBM496
- 24ABP283
- 23KBN917
- 23JBR304
- 23IBU169
- 23IBH841
- 23FBH149
- 23EBL017
- 23CBP523
- 23BBF825
- 23BBF826
- 22JBL437
- 22IBA578
- 22IBA287
- 22GBI511
- 22GBH553
- 26FBR970
- 26EBL570
- 26DBL401
- 26CBD787
- 25LBB786
- 25JBQ411
- 25JBH229
- 26DBQ234
- 25GMA962
- 25CMJ170
- 26EBH822
- UDI-DI
- 10195327270360
- 40195327270361
- Lot
- 23HBB258
- UDI-DI
- 10195327013042
- 40195327013043
- 10195327112011
- 40195327112012
- 10889942106240
- 40889942106241
- 10198459723025
- 40198459723026
- 10195327482749
- 40195327482740
- 10195327663155
- 40195327663156
- 10193489832686
- 40193489832687
- Lot
- 22HMA400
- 23GBS783
- 22HMD080
- 26CMG313
- 25KMB622
- 24EDB134
- 23IBL172
- UDI-DI
- 10889942295234
- 40889942295235
- 10193489514001
- 40193489514002
- 10195327170813
- 40195327170814
- Lot
- 22HME611
- 23GMI728
- 23EME909
- 23CMG752
- 23CMB449
- 23AMI951
- 22KMD941
- 22JMC071
- 22FMD388
- 23HMA901
- 23HMA420
- 23GBH079
- 23FBB663
- 23DBS195
- 22LBG199
- UDI-DI
- 10198459756368
- 40198459756369
- 10198459200632
- 40198459200633
- 10198459442094
- 40198459442095
- 10198459656316
- 40198459656317
- Lot
- 26EBN238
- 25GBC553
- 25FBA082
- 25EBP462
- 25DBU966
- 25CBS315
- 25JBB880
- 25HBF280
- 26CBK932
- 26BBT826
- 26BBT935
- 26EBG096
- 26DBM677
Details
- Company began the recall
- Sold in
US Nationwide.
- Event ID
- 99739
- Recall numbers
- Z-3265-2026 to Z-3269-2026
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Contamination
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
