Vero Biotech recalls
Vero Biotech appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2023-12-27.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 3 |
|---|---|
| Published | 2021-06-30 to 2023-12-27 |
| By agency | FDA Device (3) |
| By classification | Class I (2), Class II (1) |
| By status | completed (1), ongoing (1), terminated (1) |
| Distribution named in notices | AZ, FL, IL, TX, US |
Recalls
- VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01
FDA Device · Class II · 2023-12-27 · Vero Biotech
Reason: Cassette did not meet an 1n-process flow criterion. - GENOSYL DS (Delivery System) console, for use as a vasodilator
FDA Device · Class I · 2021-10-06 · Vero Biotech
Reason: Manufacturing defect involving reversal of the inlet and outlet gas lines, resulting in delivery of nitrogen dioxide (NO2) instead of nitric oxide (NO). - GENOSYL DS
FDA Device · Class I · 2021-06-30 · Vero Biotech
Reason: Reports received of NO measured below desired dose during transition between primary console and backup console since Software Version 2.2.3 was uploaded to consoles in the field.