Drug recall
Design Options¿ / Epidural anesthesia kit (10 count carton)
FDA recall event 92523 · Class II · B. Braun Medical, Inc.
Key facts
| Event ID | 92523 |
|---|---|
| Recall numbers | Z-2002-2023, Z-2003-2023 |
| Recalling firm | B. Braun Medical, Inc. |
| Product type | Devices |
| Products | Design Options¿ / Epidural anesthesia kit (10 count carton), Perifix¿ / Epidural anesthesia kit (10 count carton) |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Kits were assembled with the incorrect Filter Straw. |
| Initiation date | Jun 5, 2023 |
| Report date | Jul 5, 2023 |
| City | Allentown |
| State | PA |
| Country | United States |
| FEI number | 2523676 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: