Cardica Recalls 55 C-Port Devices

Redwood City, CA-based Cardica has recalled 55 of its C-Port xA Distal Anastomosis systems after discovering a supplier manufacturing defect, according to the Associated Press.

The devices are used by surgeons to perform coronary artery bypass surgery. Cardica reported the voluntary recall to the SEC in a Jan. 12 filing. In addition the company said the FDA has been notified.

The defect is in a single component, though the company said it believes the defect does not pose a hazard to patients. Replacement devices are being provided.

The recall will hurt the company’s fiscal results in the fourth quarter and first quarter, according to the SEC filing. Cardica did not provide an estimate.