FDA recall, , Moderate risk
Medline Medical Convenience Kits
Medline medical convenience kits contain neurosponges with potential out-of-specification endotoxin levels.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP, of Northfield, Illinois, recalled certain Medline medical convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips because the neurosponges had potential out-of-specification levels of endotoxin. The recall began July 8, 2026, and the FDA added it to its Enforcement Report on August 21, 2026.
The kits were distributed in Arizona, California, Iowa, Idaho, Illinois, Indiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, New York, Ohio, Texas, Wisconsin, and Wyoming.
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.
Incomplete list: 137 of 146 lot codes shown.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline medical convenience kits
- UDI-DI
- 10198459558757
- 40198459558758
- 10198459372667
- 40198459372668
- 10198459258961
- 40198459258962
- 10195327123819
- 40195327123810
- Lot code
- 25JMG396
- 26AMH848
- 25FMD894
- 25JMH786
- 25KMF523
- 25KMF530
- 26CMD479
- 24ABD437
- 24ABO388
- 23EBA762
- 23HBG168
- 23KBW672
- UDI-DI
- 10193489916379
- 40193489916370
- 10889942968732
- 40889942968733
- 10195327679293
- 40195327679294
- 10198459241727
- 40198459241728
- 10193489763973
- 40193489763974
- 10195327258917
- 40195327258918
- 10198459241970
- 40198459241971
- 10888277775206
- 40888277775207
- 10195327397371
- 40195327397372
- 10195327182908
- 40195327182909
- 10195327488093
- 40195327488094
- 10198459225758
- 40198459225759
- 10198459313035
- 40198459313036
- 10198459399916
- 40198459399917
- Lot code
- 23HBC070
- 24CBA416
- 23CBS214
- 23FBC803
- 23GBU042
- 23IBO417
- 24EBH594
- 24FBQ494
- 24JBK316
- 25CDA135
- 23HBK833
- 24FBQ476
- 23EBI941
- 23HBX888
- 22KBR883
- 25JMC017
- 25KMB183
- 25AMG343
- 25DMJ252
- 23ABM594
- 23DBQ757
- 23EBL559
- 22FBC585
- 22GBO880
- 22HBN179
- 22HBU967
- 25CME312
- 25FME826
- 24IMA157
- 24IMF249
- 23EBI617
- 23GBJ097
- 23HBS862
- 23JBU735
- 23KBI060
- 23ABS340
- 23ABS768
- 23BBB045
- 23HBP969
- 22HBR343
- 22HBT245
- 22LBL269
- 24DBD707
- 24DBD912
- 24HBR037
- 24IBF556
- 24JBM973
- 23LBG405
- 25BBD293
- 25BBF473
- 25BBF871
- 25DBU804
- 25EBN687
- 25FBR466
- 25HBF447
- 25KBT345
- UDI-DI
- 10193489232394
- 40193489232395
- 10195327090111
- 40195327090112
- 10195327281250
- 40195327281251
- 10193489880564
- 40193489880565
- 10193489887631
- 40193489887632
- 10193489863994
- 40193489863995
- 10195327123451
- 40195327123452
- 10195327452490
- 40195327452491
- Lot code
- 22HMB295
- 22IMB860
- 22FMB806
- 23GMI744
- 25EBV362
- 25CMH980
- 25FMB096
- 25GMA066
- 25GMH940
- 25BMI081
- 25IMC735
- 24DME519
- 24EMG256
- 24GMJ491
- 24IMA243
- 24JMA162
- 24JMD784
- 24KMI470
- 24ABN077
- 24ABN475
- 24DBA116
- 23AMH395
- 23EMA407
- 23HBH164
- 23HBO192
- 23HBV863
- 23IBF802
- 23IBS028
- 23JBV613
- 22BME230
- 22CMA406
- 22EMB248
- 22EMI134
- 22HME564
- 22IMA455
- 22JMI068
- 22LMB601
- 24BMI624
- 24EME751
- 23AMJ022
- UDI-DI
- 10198459558764
- 40198459558765
- 10198459241956
- 40198459241957
- 10195327625689
- 40195327625680
- 10195327237011
- 40195327237012
- 10193489460254
- 40193489460255
- 10193489867381
- 40193489867382
- 10193489864007
- 40193489864008
- 10195327283179
- 40195327283170
- 10198459092725
- 40198459092726
- 10195327181338
- 40195327181339
- 10193489753301
- 40193489753302
- Lot code
- 25JMF561
- 25EDA305
- 25EDB254
- 24JMF418
- 24JMJ129
- 23HBJ773
- 23HBA720
- 23BMC930
- 23FMD505
- 23JMH313
- 23LME066
- 22CMG565
- 24BME326
- 24EMF925
- 23AMJ184
- 23EMD739
- 23IME138
- 23KMB648
- 23LMB107
- 23LMH426
- 22FMF374
- 22KMH219
- 23HMC695
- 25CMD816
- 24IMD021
- 24IME838
- 23IBJ627
- 23IBL564
- 22EDB595
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of Arizona, California, Iowa, Idaho, Illinois, Indiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, New York, Ohio, Texas, Wisconsin, Wyoming.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Quality testing problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99489
- Recall numbers
- Z-2994-2026 to Z-2997-2026
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
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
