The Recall Desk

Manufacturer

Maquet

1 recall in our database name Maquet as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
0
Severe
0
Most recent
2018-02-07

Of the 1 recalls from Maquet we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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.

1–1 of 1

  • ModerateFDA (Devices)·Z-0490-2018·2018-02-07

    Maquet Recalls Expired Hemofiltration Standard Packs for Cardiopulmonary Bypass

    Maquet is recalling 55 Hemofiltration Standard Packs distributed after their September 2015 expiration date. The units were used in extracorporeal circulation during cardiopulmonary bypass procedures.

    Product
    Hemofiltration Standard Pack including BC 60 Plus-T 8036. Part Number: 701066990. Used in extracorporeal circulation during cardiopulmonary bypass procedures lasting 6 hours or less.
    Category
    Medical Device
    Distribution
    3 states