FDA Device recall Z-1841-2021
Medline Tissue Recovery Instrument Set, Reorder #DYNJ64347A, packaged 3/case, Sterile, Rx. Convenience kit used to recover tissue, which ca…
- FDA Device
- Class II
- ongoing
- Published 2021-06-16
On 2021-06-16 the FDA classified a Class II recall of Medline Tissue Recovery Instrument Set, Reorder #DYNJ64347A, packaged 3/case, Sterile, Rx. Convenience kit used to recover tissue, which ca… by Medline Industries, citing the devices may not meet the minimum required sterility assurance level.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1841-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-04-30 |
| Published | 2021-06-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries |
| Distribution | WI |
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
The devices may not meet the minimum required sterility assurance level.
Identifiers
| code_info | GTIN (01)10193489291186, lot numbers 21CDA959, 21BDB665, 21ADA390, and 20KDC285 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1841-2021%22
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