MALLINCKRODT Adverse Event — Injury (MDR 2936999-2008-00079)
MALLINCKRODT Adverse Event — Injury (MDR 2936999-2008-00079) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MALLINCKRODT; Generic name: ENDOTRACHEAL TUBE; Manufacturer: HENEQUEN.
| Device | MALLINCKRODT |
|---|---|
| Generic name | ENDOTRACHEAL TUBE |
| Manufacturer | HENEQUEN |
| Report number | 2936999-2008-00079 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | THE COMPANY RECEIVED INFO THAT SUGGESTED THAT THE PRODUCT HAD A RING SHAPED CIRCLE AROUND THE CUFF THAT WAS STIFFER THAN THE REST OF THE CUFF AND DID NOT APPEAR TO DEFLATE PROPERLY. THE CUSTOMER REPORTED, THAT THIS WAS DISCOVERED AFTER THE PT WAS EXTUBATED AND REQUIRED A TREATMENT OF RACEMIC EPINEPHRINE DUE TO STRIDOR AND AIRWAY EDEMA. POST TREATMENT, THE PT WAS BREATHING NORMALLY AND NO FURTHER T |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →