Recall image placeholder

No image published for this recall

Ge healthcare integrated and stand-alone resuscitation systems

Official notice

16 Jun 2026

Last checked

16 Jun 2026

Medium riskHealth Canada
Watch Datex-ohmeda

An official Health Canada notice concerns Ge healthcare integrated and stand-alone resuscitation systems. GE HealthCare has become aware of a potential issue involving the air-oxygen blender knob shaft on certain (serial number specific) integrated and stand-alone Resuscitation systems. In some cases, the blender knob shaft can loosen, which can affect the delivered oxygen concentration. If this occurs, the system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient. Published 2026-06-16.

What to do now

Contact the manufacturer if you require additional information.

Recall number

82212

Official notice

2026-06-16

The hazard

GE HealthCare has become aware of a potential issue involving the air-oxygen blender knob shaft on certain (serial number specific) integrated and stand-alone Resuscitation systems. In some cases, the blender knob shaft can loosen, which can affect the delivered oxygen concentration. If this occurs, the system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

How to check if you're affected

Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.

Lots

PBWZ71728, HDJT51537, HDJU65007, HDJU65440, STPC70188, PBW24120458SA, PBWY72937, PBW26048040SA

Skus

M1112198, M1118179, 2082663-001

Other

RA RA-82212

Model Numbers

M1112198, M1118179, 2082663-001

Recall Numbers

82212

Checked manually this time?

The app watches your VIN and alerts you automatically next time — no searching, no checking back.

Turn on automatic VIN checks

Affected products

Product 1

Lot or serial number - PBWZ71728, Model or catalogue number - M1112198

Product 2

Lot or serial number - HDJT51537, Model or catalogue number - M1118179

Product 3

Lot or serial number - HDJU65007, Model or catalogue number - M1118179

Product 4

Lot or serial number - HDJU65440, Model or catalogue number - M1118179

Product 5

Lot or serial number - STPC70188, Model or catalogue number - 2082663-001

Product 6

Lot or serial number - PBW24120458SA, Model or catalogue number - M1112198

Product 7

Lot or serial number - PBWY72937, Model or catalogue number - M1112198

Product 8

Lot or serial number - PBW26048040SA, Model or catalogue number - M1112198

Risk / hazard

GE HealthCare has become aware of a potential issue involving the air-oxygen blender knob shaft on certain (serial number specific) integrated and stand-alone Resuscitation systems. In some cases, the blender knob shaft can loosen, which can affect the delivered oxygen concentration. If this occurs, the system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

Where it was sold

The source does not list specific retailers. See the official notice for where affected vehicles were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Datex-ohmeda

Manufacturer

Not provided

Phone

Not provided

Brand: Datex-ohmeda.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

82212

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

CA
Recall image placeholder

Aisys, avance, and aespire anesthesia machines

Medium riskHealth Canada2 Jul 2026
CA
Recall image placeholder

Giraffe™ omnibed™ carestation™

Medium riskHealth Canada4 Jun 2026
CA
Recall image placeholder

Carestation 620, 650 and 750

Medium riskHealth Canada10 Apr 2025
CA
Recall image placeholder

Carestation 600 and 700 series anesthesia systems

Medium riskHealth Canada9 Dec 2025
CA
Recall image placeholder

Evair

Medium riskHealth Canada9 Jul 2025
CA
Recall image placeholder

Giraffe™ omnibed carestation cs1

Critical riskHealth Canada25 Sept 2024
CA
Recall image placeholder

Giraffe omnibed carestation cs1

Medium riskHealth Canada9 Jun 2023
CA
Recall image placeholder

Aisys cs2

High riskHealth Canada13 Jun 2022
CA
Recall image placeholder

Datex-ohmeda tec-6 plus and tec 850 anesthetic vaporizors

Medium riskHealth Canada12 Dec 2024
CA
Recall image placeholder

Giraffe panda ires warmer

Medium riskHealth Canada2 Aug 2022
CA
Recall image placeholder

Aisys cs2

Medium riskHealth Canada13 Jun 2022
CA
Recall image placeholder

Avance and aespire anethiesia machines

Medium riskHealth Canada30 May 2022

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 16 Jun 2026. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.