EZY DOSE PILL PLANNER 67585WM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2019-03-11 for EZY DOSE PILL PLANNER 67585WM manufactured by Apothecary Products, Llc.

Event Text Entries

[138397059] The customer stated they pressed the friday tab on the pill planner to dispense medication into a medicine cup and the pill planner tab fell into the medicine cup along with the pills. Not realizing the tab in the cup, the customer swallowed the tab along with the pills and choked on the pill planner tab. They were able to retrieve the tab from their throat after performing the heimlich against an ottoman. The customer went to the doctor the next day and was told their throat was scratched, but should heal.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0002183416-2019-00003
MDR Report Key8408345
Report SourceCONSUMER
Date Received2019-03-11
Date of Report2019-03-11
Date of Event2019-02-15
Date Mfgr Received2019-02-18
Date Added to Maude2019-03-11
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactPAXIA HER
Manufacturer Street11750 12TH AVE S
Manufacturer CityBURNSVILLE MN 55337
Manufacturer CountryUS
Manufacturer Postal55337
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEZY DOSE PILL PLANNER
Generic NamePILL PLANNER
Product CodeNXB
Date Received2019-03-11
Model Number67585WM
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAPOTHECARY PRODUCTS, LLC
Manufacturer Address11750 12TH AVE S BURNSVILLE MN 55337 US 55337


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-03-11

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