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OXYLOG 3000 PLUS (2017-10-02)
- Starting date:
- October 2, 2017
- Posting date:
- October 27, 2017
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- Healthcare Professionals, General Public, Hospitals
- Identification number:
- RA-64966
Affected products
OXYLOG 3000 PLUS
Reason
As part of market and product monitoring, Drägerwerk AG & Co. KGaA, the parent company of Draeger Medical Canada Inc., became aware that a batch of circuit boards with potentially faulty pressure sensors has been installed over a short period in early 2017 in Oxylog 2000 plus and Oxylog 3000 plus devices.
Affected products
OXYLOG 3000 PLUS
Lot or serial number
- ASKB-022
- ASKB-023
- ASKB-025
Model or catalog number
5704833
Companies
- Manufacturer
-
DRAEGERWERK AG & CO
MOISLINGER ALLEE 53-55
LUBECK
23542
GERMANY