Health product recall

Chest Bellows- Non-Magnetic Chest Pneumograph (2020-04-22)

Starting date:
April 22, 2020
Posting date:
May 8, 2020
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-73017



Last updated: 2020-05-08

Affected Products

Chest Bellows- Non-Magnetic Chest Pneumograph

Reason

Incorrect device labelling. The chest pneumograph is not labelled as containing natural rubber latex.

Affected products

Chest Bellows- Non-Magnetic Chest Pneumograph

Lot or serial number

Not applicable.

Model or catalog number

94023

Companies
Manufacturer

Invivo, a Div. of Philips Medical Systems

12151 Research Parkway

Orlando

32826

Florida

UNITED STATES