FDA Device recall Z-2473-2019
CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189
- FDA Device
- Class II
- terminated
- Published 2019-09-11
On 2019-09-11 the FDA classified a Class II recall of CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189 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-2473-2019 |
| 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
CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189
Reason
The filter capacity is not achieved due to damage of the filter membrane.
Identifiers
| code_info | Lot # 0061620283 UDI: 04046964943294 |
|---|
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-2473-2019%22
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