Medline Tissue Recovery Instrument Set — Class II medical device recall Z-1841-2021
Ongoing recall by Medline Industries Inc, reported 2021-06-16, distributed in WI. The devices may not meet the minimum required sterility assurance level.
| Recall number | Z-1841-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2021-04-30 |
| Classified | 2021-06-09 |
| Reported by FDA | 2021-06-16 |
| Distributed | WI |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10193489291186 |
| Lot numbers | 20KDC285, 21ADA390, 21BDB665, 21CDA959 |
Product
Medline Tissue Recovery Instrument Set, Reorder #DYNJ64347A, packaged 3/case, Sterile, Rx. Convenience kit used to recover tissue, which can be used for medical research, education, or transplantation.
Reason for recall
The devices may not meet the minimum required sterility assurance level.
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-1841-2021. 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.