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Health product recall

Filtek Supreme Ultra Flowable Restorative Syringe

Starting date:
June 13, 2017
Posting date:
July 7, 2017
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-63868

Reason

Incorrect manufacturer name on secondary packaging.

Affected products

Filtek Supreme Ultra Flowable Restorative Syringe

Lot or serial number

N810567
N820103

Model or catalog number

6032A2

Companies

Manufacturer
3M ESPE Dental Products
2510 Conway Avenue
St. Paul
Minnesota
UNITED STATES