MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 1996-11-25 for BD BABY THERMOMETER UNK manufactured by Becton Dickinson.
[31724]
Glass thermometer broke while mom was taking her daughters temperature rectally. The child was taken to a hosp by paramedics, where x-rays were taken and the child was placed on antibiotics and prescribed ointments to apply to her cut.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2243072-1996-00026 |
| MDR Report Key | 52245 |
| Report Source | 04 |
| Date Received | 1996-11-25 |
| Date of Report | 1996-10-29 |
| Date of Event | 1996-10-01 |
| Date Mfgr Received | 1996-10-29 |
| Date Added to Maude | 1996-12-02 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| 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 | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BD BABY THERMOMETER |
| Generic Name | GLASS THERMOMETER |
| Product Code | FLK |
| Date Received | 1996-11-25 |
| Model Number | NA |
| Catalog Number | UNK |
| Lot Number | UNK |
| ID Number | NA |
| Operator | LAY USER/PATIENT |
| Device Availability | * |
| Device Age | UNKNOWN |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 52898 |
| Manufacturer | BECTON DICKINSON |
| Manufacturer Address | 1 BECTON DR FRANKLIN LAKES NJ 07417 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 1996-11-25 |