Pulmonx recalls Zephyr Endobronchial Valve 5.5-LP models with potentially shortened expiration dates. These devices may be used until December 8, 2024, but the correct expiration date is critical for safety.
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.
Pulmonx is recalling Zephyr Endobronchial Valve 5.5-LP models that may have incorrect expiration date labels. Using these devices beyond the correct expiration date could lead to safety risks.
The device may have been labeled with a shortened expiration date, but it can be safely used until the correct expiration date of December 8, 2024. If used beyond this date, the device may not function properly or could pose safety risks.
Patients who received the Zephyr Endobronchial Valve 5.5-LP model with the specific reference number EBV-TS-5.5-LP are most at risk if they use the device past its correct expiration date.
Check for the reference number EBV-TS-5.5-LP on the device. The specific lot number 506590-V7.0 and UDI code (01)00811907030423(10)506590V70(17)241208 are also indicators of the recalled model.
Verify the expiration date on the device label; it should not be used past December 8, 2024.
The device may have been labeled with a shortened expiration date but can be safely used until the correct expiration date of December 8, 2024.
Look for the reference number EBV-TS-5.5-LP and the specific lot number 506590-V7.0 on the device.
Check the expiration date on the device label; it should not be used past December 8, 2024.
We’ve drafted a message you can send Pulmonx to request your refund or repair — edit it as you like.
Subject: Recall Z-0235-2024 — Pulmonx Pulmonx Hello, I own a Pulmonx that is covered by recall Z-0235-2024 from Pulmonx. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
