ARGYLE Adverse Event — Malfunction (MDR 10000701)
ARGYLE Adverse Event — Malfunction (MDR 10000701) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ARGYLE; Generic name: INFANT HEEL WARMER (CHEMICAL HEAT PACK); Manufacturer: CARDINAL HEALTH, INC..
| Device | ARGYLE |
|---|---|
| Generic name | INFANT HEEL WARMER (CHEMICAL HEAT PACK) |
| Manufacturer | CARDINAL HEALTH, INC. |
| Report number | 10000701 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | NURSE WAS ACTIVATING A NEONATAL HEEL WARMER TO APPLY TO PATIENT, BUT BEFORE IT REACHED THE PATIENT THE ACTIVATED HEEL WARMER EXPLODED ON NURSE AND IN ROOM. |
| Source | openFDA MAUDE (device adverse events) |
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