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Getinge is announcing a medical device recall/field action related to packaging of QUADROX-iD Pediatric Oxygenators

December 18, 2019 Gothenburg, Sweden

Getinge is announcing a medical device recall/field action related to packaging of QUADROX-iD Pediatric Oxygenators

Getinge is announcing a global medical device recall/field action related to the packaging of QUADROX-iD Pediatric Oxygenators. To date, there are no known adverse events associated with illness or injuries related to damage to the sterile barrier. Getinge has reported to relevant authorities according to applicable regulations and the cost for the field correction and recall is not material.

The QUADROX-iD Pediatric Oxygenator is a product used in extracorporeal support. This global recall/field action is initiated due to an identified potential packaging integrity issue of the product with BIOLINE Coating. The affected QUADROX-iD Pediatric Oxygenators with BIOLINE Coating were distributed between October 31, 2017 – July 25, 2019

All concerned customers have received communication. Customers are requested to remove and return affected products for collection and destruction.

This information is released in order to inform users of mentioned Getinge products, according to standard procedure recommended by regulatory authorities.
 

Media contact:

Anna Appelqvist, Vice President Corporate Communications
Phone: +46 (0)10 335 5906
E-mail: anna.appelqvist@getinge.com

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