FDA recall, , Moderate risk
Medline and Centurion Medical Convenience Kits
Medical convenience kits containing Webcol Large Alcohol Prep Pads may not be sterile due to a contaminant.
What happened
Medline Industries, LP, of Northfield, Illinois, is recalling specific lots of Medline and Centurion medical convenience kits that contain Cardinal Health Webcol Large Alcohol Prep Pads, because the pads may not be sterile.
Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit. The recall began March 16, 2026, and the FDA added it to its Enforcement Report on April 30, 2026. The kits were distributed nationwide.
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?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline and Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads
- UDI-DI
- 10653160264965
- 00653160264968
- 2025101090
- 10653160327936
- 00653160327939
- 2025100890
- 00653160126938
- 10653160126935
- 2025103190
- 10193489195453
- 20193489195450
- 2025110590
- 2025110790
- 10888277781276
- 40888277781277
- 2025111990
- 10888277781320
- 40888277781321
- 2025112490
- 10653160304739
- 00653160304732
- 2025120990
- 10653160280101
- 00653160280104
- 2026010690
- 2026011390
- 00653160091427
- 50653160091422
- 2026021090
- 10653160290667
- 00653160290660
- 2026020690
- 2026020990
- 2026021290
- 2026021790
- 10653160355724
- 00653160355727
- 2025121990
- UDI-DI
- 10889942873890
- 40889942873891
- 10653160382638
- 00653160382631
- 2025101090
- 10653160384045
- 00653160384048
- 2025112090
- 10653160367598
- 00653160367591
- 2025111890
- 10653160376071
- 00653160376074
- 2025120190
- 2026010290
- 2026010790
- 2026012090
- 2026012390
- 10653160363163
- 00653160363166
- 2026010690
- Lot code
- 26BBC230
Some entries omit identifying details. Check the notice to confirm which units are affected.
Medline medical convenience kits, containing Webcol Large Alcohol Prep Pads
- UDI-DI
- 10193489197679
- 20193489197676
- 2025101301
- 2025113001
- 10193489195804
- 20193489195801
- 2025120390
- 2026022390
Medline or Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads
- UDI-DI
- 10653160293798
- 00653160293791
- 2025102390
- 10653160259213
- 00653160259216
- 10653160319160
- 00653160319163
- 2025110790
- 10653160322511
- 00653160322514
- 2025111890
- 00653160194210
- 10653160194217
- 2025112690
- 10888277732537
- 20888277732534
- 2025120190
- 2025122690
- 2026010590
- 2026010990
- 2026011990
- 2026012990
Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: Latex Free General Purpose Tray, Medline Kit SKU 75670
- UDI-DI
- 00653160095890
- 10653160095897
- 2025102290
Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: Dermatology Shave Kit, Medline Kit SKU SK395
- UDI-DI
- 10653160280644
- 00653160280647
- 2025102090
- 2026010990
Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: Universal Central/Art Line Insertion Kit, Medline Kit SKU ART155A
- UDI-DI
- 10653160316459
- 00653160316452
- 2025100890
- 2026011290
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Sterility 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
- 98692
- Recall numbers
- Z-2039-2026 to Z-2045-2026
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



