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