The Recall Desk

Manufacturer

Vero Biotech, LLC

3 recalls in our database name Vero Biotech, LLC as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
2
Most recent
2023-12-27

Of the 3 recalls from Vero Biotech, LLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (67%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–3 of 3

  • ModerateFDA (Devices)·Z-0564-2024·2023-12-27

    Vero Biotech GENOSYL DS cassette recalled for manufacturing flow defect

    Vero Biotech is recalling GENOSYL DS Generation 3 cassettes that failed to meet manufacturing flow specifications. The recall affects 2 units distributed in Arizona and Florida.

    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
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2587-2021·2021-10-06

    GENOSYL DS vasodilator console recalled for reversed gas lines defect

    Vero Biotech recalled 3 GENOSYL DS consoles for a manufacturing defect that reverses gas inlet and outlet lines, causing delivery of toxic nitrogen dioxide instead of therapeutic nitric oxide.

    Product
    GENOSYL DS (Delivery System) console, for use as a vasodilator.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1863-2021·2021-06-30

    Nitric Oxide Delivery System Dosing Deficiency During Console Transitions

    GENOSYL DS Nitric Oxide Delivery System is recalled for delivering below-intended doses during transitions between primary and backup consoles following a software update.

    Product
    GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860
    Category
    Medical Device
    Distribution
    Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

VERO Biotech LLC

Source: Wikidata (Q140207441), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.