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Ezy Dose 67661/HK67661/67661NIRecalls & reported problems

Apothecary Products, LLC · EZY-CUT TABLET CUTTER · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00025715676616), received between Mar 28, 2021 and Mar 28, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Insufficient Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 28, 2021Insufficient Device Problem Information; Insufficient Device Problem Information

    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.

    Patient problems: Insufficient Information

    MAUDE report 11580345 ↗

Other Pill Crusher/Cutter devices

All Pill Crusher/Cutter devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.