MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1996-08-16 for THERMOMETER * manufactured by Beckton Dickinson Products.
[24340]
Customer returned a basal thermometer which had been received broken. Pharmacy reordered two (2) and one came in broken, the other was not. Upon further inspection of non-broken thermometer, it was noticed that they are very difficult to remove from packaging and could break also in just trying to remove from its holder.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1009734 |
| MDR Report Key | 35652 |
| Date Received | 1996-08-16 |
| Date of Report | 1996-08-05 |
| Date of Event | 1996-08-01 |
| Date Added to Maude | 1996-08-22 |
| 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 |
| Reporter Occupation | PHARMACIST |
| 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 | THERMOMETER |
| Generic Name | THERMOMETER |
| Product Code | FLK |
| Date Received | 1996-08-16 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | LAY USER/PATIENT |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 37079 |
| Manufacturer | BECKTON DICKINSON PRODUCTS |
| Manufacturer Address | 1 BECTON DRIVE FRANKLIN LAKES NJ 07417 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1996-08-16 |