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Health product recall

KimVent Microcuff Subglottic Suctioning Endotracheal Tube (2014-11-21)

Starting date:
November 21, 2014
Posting date:
December 5, 2014
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-42721

Recalled Products

KimVent Microcuff Subglottic Suctioning Endotracheal Tube

Reason

It was identified that the inflation line may detach from the endotracheal tubes during use.

Affected products

KimVent Microcuff Subglottic Suctioning Endotracheal Tube

Lot or serial number

AA4097V01

AA4111V02

AA4134V02

Model or catalog number

13221

13222

Companies
Manufacturer

Kimberly-Clark

1400 Holcomb Bridge Road,

Roswell

30076

Georgia

UNITED STATES