Health product recall

FABIUS SYSTEM (2021-07-01)

Starting date:
July 1, 2021
Posting date:
July 16, 2021
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-76025

Last updated: 2021-07-15

Affected Products

A. FABIUS TIRO ANESTHESIA SYSTEM
B. FABIUS GS ANESTHESIA SYSTEM
C. FABIUS GS PREMIUM SYSTEM
D. FABIUS MRI

Reason

Draeger is providing new reprocessing instructions for all Fabius-type anesthesia machines.

Affected products

A. FABIUS TIRO ANESTHESIA SYSTEM

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

8606000
8608400

Companies
Manufacturer
Draegerwerk AG & Co. KGaA
Moislinger Allee 53-55
Lübeck
23542
GERMANY

B. FABIUS GS ANESTHESIA SYSTEM

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

8604700

Companies
Manufacturer
Draegerwerk AG & Co. KGaA
Moislinger Allee 53-55
Lübeck
23542
GERMANY

C. FABIUS GS PREMIUM SYSTEM

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

8607000

Companies
Manufacturer
Draegerwerk AG & Co. KGaA
Moislinger Allee 53-55
Lübeck
23542
GERMANY

D. FABIUS MRI

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

8607300

Companies
Manufacturer
Draegerwerk AG & Co. KGaA
Moislinger Allee 53-55
Lübeck
23542
GERMANY