FDA Adverse Event Injury Summary report: N

EZY-DOSE

MDR report key: 11580345 · Received March 28, 2021

Report

Report Number
0002183416-2021-00001
Event Type
Injury
Date Received
March 28, 2021
Date of Event
January 22, 2021
Report Date
March 28, 2021
Manufacturer
APOTHECARY PRODUCTS LLC
Product Code
OHY
UDI-DI
00025715676616
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

APOTHECARY PRODUCTS LLC., RECEIVED A REPORT FROM THE CUSTOMER ALLEGES SHE HAD A LACERATION TO HER THUMB WHILE CUTTING A PILL WITH OUR PRODUCT. SHE WAS TREATED AT THE EMERGENCY ROOM AND HER CUT WAS TREATED. THE PATIENT BOUGHT OUR PRODUCT WITH OUR CUSTOMER PUBLIX. OUR PRODUCT WARNING, STATES THAT THE BLAD IS SHARP STAINLESS STEEL BLADE, DIRECT CONTACT WITH THE BLADE NEEDS TO BE AVOIDED AS IT IS VERY SHARP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
477615 EZY-DOSE PILL CUTTER OHY APOTHECARY PRODUCTS LLC 67661 150O 00025715676616

Patients

Seq Age Sex Outcome Treatment
1