EasyTouch 63116102Recalls & reported problems
Mhc Medical Products, LLC · ET 31G 5/16 IN 1cc/mL Dual Mark U-100 Syr [INDV] [600ct] · 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 MHC1631161022), received between Jun 16, 2026 and Jun 16, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Collapse” (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.
Reports received per month
Most reported problems
Device problems
- Collapse1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 16, 2026Collapse
I WAS ON ZEPBOUND SINGLE VIALS. THEY SEND EASY- TOUCH NEEDLES. 31 GAUGE 5/16 LOT NUMBER 76241, ITEM 63116102, MANUFACTURED 11-05-2025, EXP-11-04-2030. THESE NEEDLES BEND WHEN YOU INSERT THEN INTO THE VIAL. SOMETIMES THEY BEND LEFT OR RIGHT AND SOMETIMES THEY JUST CRUMPLE ON THEMSELVES. DURING MY MOST RECENT INJECTION THE NEEDLE BROKE OFF UNDER MY SKIN IN THE LOWER ABDOMEN. I WENT TO THE EMERGENCY ROOM. BOTH AN X RAY AND ULTRASOUND WAS DONE AND THEY CONFIRMED A RETAINED FRAGMENT OF THE NEEDLE AND PLACED ME ON ANTIBIOTICS. I HAVE AN APPOINTMENT WITH GENERAL SURGEON (B)(6) IN APPROXIMATELY ONE WEEK, I HAD REPORTED THIS EARLIER TO SOMEONE AT (B)(6) BUT CANNOT TELL YOU WHO. THIS TIME I SPOKE WITH (B)(6) AT (B)(6).
Patient problems: Foreign Body In Patient
MAUDE report 25522676 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.