Centurion medical procedure kits — Class II medical device recall Z-2028-2026
Ongoing recall by Medline Industries, LP, reported 2026-05-06. During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medlin
| Recall number | Z-2028-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-03-19 |
| Classified | 2026-04-30 |
| Reported by FDA | 2026-05-06 |
| Quantity | 3,000 kits |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10653160323068, 40653160323069 |
| Lot numbers | 21ABI942, 21CBL756, 21EBR576, 21GBB532, 21IBM298, 21IBM495, 22ABU694, 22DBP674, 22GBL079, 22HBC645, 23CBO045, 23FBW067, 23IBS518, 23JBY390, 24ABW463, 24EBU727, 24HBT740, 24JBW176, 24LBO080, 25BBD132, 25DBH934, 25GBB222, 25IBK286, 25LBS129, 26ABG606 |
Product
Centurion medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SURGICAL ENT PREP KIT, Medline Kit Number/SKU MNS11715
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2028-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.