FDAClass IIDecember 27, 2023

Vero Biotech Genosyl DS recall

VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric oxide (NO) for inhalation at…

Why was Vero Biotech Genosyl DS recalled?

Cassette did not meet an 1n-process flow criterion.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Code: W-0001-2023, Cassette serial numbers: GA01T707, GA01T108

Product
VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric oxide (NO) for inhalation at…
Recalling firm
Vero Biotech, LLC
Quantity
2 cassettes
Distribution
US: AZ and FL
Recall date
December 27, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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