FDA Device recall Z-2469-2019
CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183
- FDA Device
- Class II
- terminated
- Published 2019-09-11
On 2019-09-11 the FDA classified a Class II recall of CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183 by B Braun Medical, citing the filter capacity is not achieved due to damage of the filter membrane.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2469-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-10 |
| Published | 2019-09-11 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | B Braun Medical |
| Distribution | AL, CA, FL, GA, IL, MN, MO, NC, PA, TX |
Product
CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183
Reason
The filter capacity is not achieved due to damage of the filter membrane.
Identifiers
| code_info | Lot # 0061536635 Exp: 10/31/2018 Lot # 0061620271 Exp:11/30/2019 UDI: 04046964941337 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2469-2019%22
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