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EasyTouch 802015Recalls & reported problems

Mhc Medical Products, LLC · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI MHC18020151), received between Jun 14, 2022 and Jun 14, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect Measurement” (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

  • Incorrect Measurement1

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.

  • MalfunctionJun 14, 2022Incorrect Measurement; Incorrect Measurement

    CUSTOMER REPORTED THAT THE SHAPE OF THE PLUNGER OF THE SYRINGE PROVIDED IN THE ANCILLARY CONVENIENCE KIT IS CAUSING AN INACCURATE MEASUREMENT OF VACCINE. THE CUSTOMER STATED THAT THEY MEASURED THE SYRINGES AGAINST OTHERS USED IN THE PAST AND CLAIM THAT THERE IS A DISPARITY IN THE ACCURACY OF THE DOSAGES. CUSTOMER STATED THAT WHILE DRAWING UP 6 DOSAGES, MEDICATION WAS STILL LEFT IN THE VIAL, FOR EXAMPLE THE DOSAGE SHOULD BE 0.3 BUT DUE TO THE EXTRA STOPPER PULL RESULTED IN A DOSAGE AMOUNT OF LESS THAN 0.3.

    Patient problems: Insufficient Information

    MAUDE report 14687625 ↗

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