Redwood City, CA, United States
Pulmonx, Corp. recalls
1 recall recorded since 2018, most recently on 31 August 2023. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 31 August 2023
- Reason
- 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
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0235-2024
- Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.