MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-14 for PILL CRUSHER manufactured by Unk.
[100317964]
It simply did not work. Upon crushing the pills on first use, the top inside projector collapsed, therefore unable to crush the pill. Incident location: home/apartment/condominium. Pill crusher, flents, ezy-dose, (b)(6). I certify that i have reviewed the report and that the info provided in this report is true: yes.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5075275 |
| MDR Report Key | 7273442 |
| Date Received | 2018-02-14 |
| Date of Report | 2018-02-03 |
| Date of Event | 2018-02-02 |
| Date Added to Maude | 2018-02-15 |
| 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 | 3 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | PILL CRUSHER |
| Generic Name | PILL CRUSHER |
| Product Code | OHY |
| Date Received | 2018-02-14 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-02-14 |