Class II — B. Braun Medical, Inc.
| Recalling firm | B. BRAUN MEDICAL INC. |
|---|---|
| Registered facility | View this company's 5 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The filter capacity is not achieved due to damage of the filter membrane. |
| Product | ES1827KN SPINAL/EPIDURAL TRAY NRFIT Catalog # 339115 |
| Quantity | 200 units |
| Distribution | CA FL MO TX MN AL GA NC IL PA |
| Initiated | 2019-07-10 |
| Classified | 2019-09-05 |
| Terminated | 2020-08-21 |
| Recall number | Z-2467-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — B. Braun Medical, Inc. (Z-2467-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83478/
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