EZYDOSE PILL CRUSHER 71091

MAUDE Adverse Event Report

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.

MAUDE Entry Details

Report Number0002183416-2019-00004
MDR Report Key8664286
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2019-06-03
Date of Report2019-06-03
Date of Event2019-05-14
Date Mfgr Received2019-05-15
Date Added to Maude2019-06-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS PAXIA HER
Manufacturer Street11750 12TH AVE. S
Manufacturer CityBURNSVILLE MN 55337
Manufacturer CountryUS
Manufacturer Postal55337
Manufacturer Phone9528088364
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEZYDOSE PILL CRUSHER
Generic NamePILL CRUSHER
Product CodeOHY
Date Received2019-06-03
Returned To Mfg2019-05-31
Model Number71091
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerAPOTHECARY PRODUCTS, LLC
Manufacturer Address11750 12TH AVE S. BURNSVILLE MN 55337 US 55337


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-06-03

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