KIMBERLY-CLARK TRACH CARE PRODUCTS Adverse Event — Malfunction (MDR 8030647-2008-00002)
KIMBERLY-CLARK TRACH CARE PRODUCTS Adverse Event — Malfunction (MDR 8030647-2008-00002) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: KIMBERLY-CLARK TRACH CARE PRODUCTS; Generic name: ENDOTRACHEAL TUBE ADAPTERS; Manufacturer: AVENT S.A. DE C.V..
| Device | KIMBERLY-CLARK TRACH CARE PRODUCTS |
|---|---|
| Generic name | ENDOTRACHEAL TUBE ADAPTERS |
| Manufacturer | AVENT S.A. DE C.V. |
| Report number | 8030647-2008-00002 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional, User facility |
| Narrative | THE USER FACILITY REPORTED TO THE MFR THAT DURING TRACHEA SUCTIONING PROCEDURE, THE SUCTION CATHETER DISCONNECTED FROM THE VALVE AND REMAINED IN THE ENDOTRACHEAL TUBE. IT WAS REMOVED WITH A CLAMP. THERE WAS NO REPORT OF INJURY OR ADVERSE CONSEQUENCES AS A RESULT OF THE DISCONNECTION. KIMBERLY-CLARK HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED, BUT IS RELAYING THE INFO THAT WAS PROVIDED BY TH |
| Source | openFDA MAUDE (device adverse events) |
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