The Recall Desk

Manufacturer

Datex-Ohmeda, Inc.

26 recalls in our database name Datex-Ohmeda, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
26
Critical
1
Severe
17
Most recent
2026-06-24

Of the 26 recalls from Datex-Ohmeda, Inc. we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 17 (65%) 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.

26–26 of 26

  • HighFDA (Devices)·Z-2266-2018·2018-06-27

    Datex-Ohmeda CARESCAPE R860 Ventilators Recalled for Display Processor Failure

    Datex-Ohmeda is recalling CARESCAPE R860 ventilators with software version 10SP05 because the display processor may experience unexpected failure.

    Product
    CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The CARESCAPE R860 ventilator is designed to provide mechanical ventilation or support to neonatal, pediatric, and adult patients weighing 0.25 kg and above. The CARESCAPE R860 ventilator is a microprocess
    Category
    Medical Device
    Distribution
    Distributed nationwide