MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2019-06-03 for EZYDOSE PILL CRUSHER 71091 manufactured by Apothecary Products, Llc.
Report Number | 0002183416-2019-00004 |
MDR Report Key | 8664286 |
Report Source | COMPANY REPRESENTATIVE,CONSUM |
Date Received | 2019-06-03 |
Date of Report | 2019-06-03 |
Date of Event | 2019-05-14 |
Date Mfgr Received | 2019-05-15 |
Date Added to Maude | 2019-06-03 |
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 | MS PAXIA HER |
Manufacturer Street | 11750 12TH AVE. S |
Manufacturer City | BURNSVILLE MN 55337 |
Manufacturer Country | US |
Manufacturer Postal | 55337 |
Manufacturer Phone | 9528088364 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | EZYDOSE PILL CRUSHER |
Generic Name | PILL CRUSHER |
Product Code | OHY |
Date Received | 2019-06-03 |
Returned To Mfg | 2019-05-31 |
Model Number | 71091 |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
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. Required No Informationntervention | 2019-06-03 |