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Heliomolar Refill (Cavifil)
- Starting date:
- July 20, 2017
- Posting date:
- August 15, 2017
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-64218
Reason
Specific product codes and lots of Heliomolar, delivery form Cavifil only, may exhibit soft and sticky consistency and therefore may cause unexpected handling for the user during packing and contouring..
Affected products
Heliomolar Refill (Cavifil)
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
541501AN
541502AN
541503AN
Companies
- Manufacturer
-
Ivoclar Vivadent AG
Bendererstrasse #2
Schaan
9494
LIECHTENSTEIN