MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-23 for PILL BOTTLE manufactured by Unk.
[125283900]
The containers used by my pharmacy for prescription pills are markedly inferior. The threads in the body and the cap are poor quality, resulting in cross-threading, or failure of the caps to completely screw down. If the containers are dropped from the overhead cabinet to the sink countertop, or from my waist to the floor, the caps falls off, spilling all the pills. The pharmacy is (b)(6). They were advised of the problem, but continue using the same container. I can provide a sample of the container. The product is not compounded; the product was not over-the-counter.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5080802 |
| MDR Report Key | 8000066 |
| Date Received | 2018-10-23 |
| Date of Report | 2018-10-11 |
| Date of Event | 2018-10-11 |
| Date Added to Maude | 2018-10-24 |
| 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 BOTTLE |
| Generic Name | DISPENSER, SOLID MEDICATION |
| Product Code | NXB |
| Date Received | 2018-10-23 |
| 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 | 1. Other | 2018-10-23 |