Health product recall

BioPince Automatic Full Core Biopsy Instrument (2019-12-03)

Starting date:
December 3, 2019
Posting date:
December 20, 2019
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-71935

Last updated: 2019-12-20

Affected Products

BioPince Automatic Full Core Biopsy Instrument

Reason

A data-entry error into the labelling software resulted in the correct box label (16ga X 15cm) but an incorrect tray label (18ga X 15cm).

Affected products

BioPince Automatic Full Core Biopsy Instrument

Lot or serial number

11277175

Model or catalog number

370-1580-01

Companies
Manufacturer
Argon Medical Devices Inc.
1445 Flat Creek Road
Athens
75751
Texas
UNITED STATES