GENOSYL DS Cassette (Vero Biotech) – Flow Criterion Issue (2023)
This recall may present a risk under certain conditions.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric oxide (NO) for inhalation at the point of use
Brand
Vero Biotech, LLC
Lot Codes / Batch Numbers
Lot Code: W-0001-2023, Cassette serial numbers: GA01T707, GA01T108
Products Sold
Lot Code: W-0001-2023, Cassette serial numbers: GA01T707, GA01T108
Vero Biotech, LLC is recalling VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates a due to Cassette did not meet an 1n-process flow criterion.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Cassette did not meet an 1n-process flow criterion.
Recommended Action
Per FDA guidance
VERO BIOTECH issued an URGENT: MEDICAL DEVICE REMOVAL notice to its consignees on 11/17/2023 via email, The notice explained the issue and advised the consignee of the removal of the device from their possession on 11/03/2023.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, FL
Page updated: Jan 10, 2026