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Health product recall

ENDOFLATOR TUBING (WITH FILTER) (2017-10-11)

Starting date:
October 11, 2017
Posting date:
October 20, 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-64910

Affected products

ENDOFLATOR TUBING (WITH FILTER)

Reason

A labeling error on the individual pouches of some of the Karl Storz Endoflator high-flow insufflation tubing (with filter), catalog #20400161s/10. The affected boxes are correctly labeled with #20400161s/10. Inside the box, the 10 individual pouches of the 20400161s Endoflator tubing were mislabeled with "catalog number 20400162s, high-flow insufflation tubing (with filter) for 26432020-1 Thermoflator". This error occurred with lot #129241 only. However, not all boxes with lot #12941 are impacted.

Affected products

ENDOFLATOR TUBING (WITH FILTER)

Lot or serial number

129241

Model or catalog number

20400161S/10

Companies
Manufacturer
Karl Storz Gmbh & Co. Kg
Mittelstrasse 8
Tuttlingen
78532
GERMANY