Pulmonx, Corp.: Medical Device Recall in 2023 - (Recall #: Z-0235-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 31, 2023

Date Posted: November 15, 2023

Recall Number: Z-0235-2024

Event ID: 93179

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.

Status: Ongoing

Product Quantity: 144

Code Information:

UDI: (01)00811907030423(10)506590V70(17)241208, Lot: 506590-V7.0

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated