Drug recall
Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP
FDA recall event 93179 · Class II · Pulmonx, Corp.
Key facts
| Event ID | 93179 |
|---|---|
| Recall numbers | Z-0235-2024 |
| Recalling firm | Pulmonx, Corp. |
| Product type | Devices |
| Products | Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Endobronchial implant devices may have been labeled with a shortened expiration date but they can be used until the correct expiration date: 08 December 2024. |
| Initiation date | Aug 31, 2023 |
| Report date | Nov 15, 2023 |
| City | Redwood City |
| State | CA |
| Country | United States |
| FEI number | 3007797756 |
At a glance
- 1–9 Products in this recall
- 1–9 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: