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Whole-Body Hyperthermia Device Heckel-HT2000 (2015-04-28)
- Starting date:
- April 28, 2015
- Posting date:
- June 26, 2015
- 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-53888
Recalled Product
A. Whole-Body Hyperthermia Device Heckel-HT2000
Reason
The whole-body hyperthermia device HT-2000 was sold into Canada without holding a valid medical device licence.
Affected products
A.Whole-Body Hyperthermia Device Heckel-HT2000
Lot or serial number
All Serial Numbers
Model or catalog number
FEBROSKRIPT2000
HT2000
Companies
- Manufacturer
-
HECKEL MEDIZINTECHNIK GMBH
OLGASTRASSE 25, 73728 ESSLINGEN
Hamburg
GERMANY