MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1999-03-04 for NEO-THERM SKIN TEMP SENSOR * STS201 manufactured by Smiths Industries Medical Systems, Inc..
[130925]
Failed to register temperature.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1015851 |
| MDR Report Key | 213146 |
| Date Received | 1999-03-04 |
| Date of Report | 1999-03-03 |
| Date Added to Maude | 1999-03-10 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NEO-THERM SKIN TEMP SENSOR |
| Generic Name | TEMPERATURE SENSOR |
| Product Code | HCS |
| Date Received | 1999-03-04 |
| Model Number | * |
| Catalog Number | STS201 |
| Lot Number | 1521 |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 206808 |
| Manufacturer | SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. |
| Manufacturer Address | 15 KIT ST. KEENE NH 03431 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1999-03-04 |