Connector, Catheter

FDA product code GCD · Class 1 · General, Plastic Surgery

244

Registered devices

Adverse events

Recalls

510(k) clearances

Devices with this code

Date	Firm	Reason
2022-08-16	Cook Incorporated	Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of
2017-04-21	Teleflex Medical	Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
2017-04-21	Teleflex Medical	Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
2017-04-21	Teleflex Medical
2017-04-21	Teleflex Medical	Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
2005-11-17	Becton Dickinson & Company	The catheter connector could not be sufficiently tightened to secure the catheter tubing.
2005-11-17	Becton Dickinson & Company	The catheter connector could not be sufficiently tightened to secure the catheter tubing.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.