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Health product recall

Kwik-Stik 939p - Actinomyces Odontolyticus

Starting date:
March 1, 2017
Posting date:
April 4, 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-62892

Reason

The product is being recalled because it is mislabelled. The actual organism contained with the product is Eggerthella lenta. It is supposed to contain Actinomyces odontolyticus.

Affected products

Kwik-Stik 939p - Actinomyces Odontolyticus

Lot or serial number

939-47-2

Model or catalog number

0939P

Companies

Manufacturer
Microbiologics, Inc.
200 Cooper Ave. N
St. Cloud
56303
Minnesota
UNITED STATES