Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zephyr Endobronchial Valve (EBV) 5.5-LP Recalled by Pulmonx, Corp. Due to Endobronchial implant devices may have been labeled with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pulmonx, Corp. directly.
Affected Products
Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP
Quantity: 144
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 22 states: AZ, AR, CO, FL, IL, IA, MA, MI, NV, NJ, NY, NC, OH, OK, OR, PA, TN, TX, VA, WA, WV, WI
About Pulmonx, Corp.
Pulmonx, Corp. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report