MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2019-07-17 for EZY DOSE PILL PLANNER 67585WM manufactured by Apothecary Products, Llc.
Report Number | 0002183416-2019-00006 |
MDR Report Key | 8800357 |
Report Source | CONSUMER |
Date Received | 2019-07-17 |
Date of Report | 2019-07-17 |
Date of Event | 2019-06-16 |
Date Mfgr Received | 2019-06-17 |
Date Added to Maude | 2019-07-17 |
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 | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | PAXIA HER |
Manufacturer Street | 11750 12TH AVE S |
Manufacturer City | BURNSVILLE MN 55337 |
Manufacturer Country | US |
Manufacturer Postal | 55337 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | EZY DOSE PILL PLANNER |
Generic Name | PILL PLANNER |
Product Code | NXB |
Date Received | 2019-07-17 |
Returned To Mfg | 2019-07-02 |
Model Number | 67585WM |
Device Availability | R |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | APOTHECARY PRODUCTS, LLC |
Manufacturer Address | 11750 12TH AVE S BURNSVILLE MN 55337 US 55337 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-07-17 |