ClearanceBrief
Recall Z-1267-2010 ยท CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

Philips Healthcare Inc.

Spanish Capnogard 1265, Respironics/Philips product. Intended to be used for monitoring end tidal CO2 and respiration rate in all critical monitoring environments.

DateApr 8, 2010 (initiated Nov 19, 2009)
StatusTerminated
ReasonPower cords' prongs may crack or fail -- Philips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords used with medical devices may be defective in that the power cord's prongs may crack and fail at/or inside the plug. Potential for burns or electrical shock.
Root causeNonconforming Material/Component
ActionPhilips was notified that FDA is investigating whether certain types of Electri-Cord Manufacturing Company power cords used with medical devices may be defective in that the power cord's prongs may crack and fail at/or inside plug. The issue affects medical device power cords equipped with a plug that has a prong and ground-pin insert design and a black plastic bridge connecting the terminal prongs on the plug ("taller bridge" design). Medical device power cords that do not have a black bridge connecting the terminal prongs on the plug are not affected. Urgent Medical Device Correction let
Quantity14
DistributionWorldwide Distribution -- UNITED STATES, ALGERIA, ARGENTINA, Aruba, AUSTRALIA, BAHRAIN, BANGLADESH, BELGIUM, BRAZIL, CAMBODIA, CANADA, CHILE, CHINA, COLOMBIA, COSTA RICA, CROATIA, CZECH REPUBLIC, Denmark, ECUADOR, EGYPT, FINLAND, FRANCE, GERMANY, GREECE, GUATEMALA, HONG KONG, HUNGARY, INDIA, INDONES
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K910019NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON
Novametrix Medical Systems, Inc., Mar 26, 1991