Universal connector 1/4 x 1/4 Fr 24-36
REDAX SPA · Model 10507 · UDI-DI 08034139290959
GCD
Prescription
8
510(k) clearances
53
Adverse events
7
Recalls
70
Facilities
Description
Fittinig device designed to facilitate the connection of the tubes/drainage catheters.
Recalls
| 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 affected devices may |
| 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. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.