The Recall Desk

FDA (Devices) recall action 93548

Maquet Cardiovascular, LLC recalled 2 products on 2024-01-24

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2024-01-24
Critical
0
Units

Why these products were recalled

Express chest drains are pre-packaged with sterile water syringes which have bene recalled. If the device is not kept in an upright position, the patient may be exposed to infectious material. Subsequent hazards include but are not limited to infection, abscess, sepsis, and death.

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

  • SevereFDA (Devices)··2024-01-24

    Express Chest Drains Recalled for Infection Risk from Recalled Syringes

    Maquet Cardiovascular is recalling Express chest drains pre-packaged with recalled sterile water syringes. If not kept upright, patients may be exposed to infectious material, risking infection, abscess, sepsis, and death.

    Product
    Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection
    Category
    Distribution
    0 states
  • SevereFDA (Devices)··2024-01-24

    FDA Recalls Express Chest Drain Blood Recovery Units Over Infection Risk

    Maquet Cardiovascular is recalling Express chest drain units with defective sterile water syringes. If not kept upright, patients risk exposure to infectious material that may cause infection, abscess, sepsis, or death.

    Product
    Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit
    Category
    Distribution
    0 states