FDA Device recall Z-2002-2023
Perifix¿ / Epidural anesthesia kit (10 count carton)
- FDA Device
- Class II
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class II recall of Perifix¿ / Epidural anesthesia kit (10 count carton) by B Braun Medical, citing kits were assembled with the incorrect Filter Straw.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2002-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-06-05 |
| Published | 2023-07-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | B Braun Medical |
| Distribution | US |
Product
Perifix¿ / Epidural anesthesia kit (10 count carton)
Reason
Kits were assembled with the incorrect Filter Straw.
Identifiers
| code_info | Model No. 332217, 332097, 332220, 332078; GTIN: 04046964178283, 04046964177361, 04046964177361, 04046964178320, 0404696…Model No. 332217, 332097, 332220, 332078; GTIN: 04046964178283, 04046964177361, 04046964177361, 04046964178320, 04046964177200; Lot No. 0061850767, 0061855339, 00618553400061858554, 0061837264. |
|---|
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-2002-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.