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LeoniPlus and LeoniPlus with HFO (2014-11-05)
- Starting date:
- November 5, 2014
- Posting date:
- November 21, 2014
- 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-42219
Recalled products
- LeoniPlus
- LeoniPlus with HFO
Reason
If contrary to the instruction for use, the display is cleaned with liquids instead of wiping with an approved cleaning agent, ingress of such liquids may lead to malfunction of the keypad identified as a permanent or a mission function of the keys. Do not use machine.
Affected products
A. LeoniPlus
Lot or serial number
Not applicable
Model or catalog number
- 0217001
Companies
- Manufacturer
-
Heinen + Löwenstein GmbH & Co.
KG, Arzbacher Straße 80,
Bad Ems
56130
GERMANY
B. LeoniPlus with HFO
Lot or serial number
Not applicable
Model or catalog number
- 0217002
Companies
- Manufacturer
-
Heinen + Löwenstein GmbH & Co.
KG, Arzbacher Straße 80,
Bad Ems
56130
GERMANY