# FDA recall Z-0235-2024

> **Pulmonx, Corp.** · Class II · device recall initiated 2023-08-31.

## Product

Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP

## 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.

## Distribution

US: TN, WV, AR, PA, VA, NC, IL, IA, MA, NY, NJ, WA, CO, OR, MI, FL, OH, TX, OK, AZ, NV, WI

## Key facts

- **Recall number:** Z-0235-2024
- **Recalling firm:** Pulmonx, Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-31
- **Report date:** 2023-11-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Redwood City, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0235-2024

## Citation

> AI Analytics. FDA recall Z-0235-2024. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-0235-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*