Equashield Equashield Syringe Unit (UDI 07290013484024)Recalls & reported problems

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 07290013484024), received between Mar 10, 2025 and Mar 10, 2025 — classified as 1 malfunction.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Patient problems

No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

MalfunctionMar 10, 2025
WHILE PULLING VINCRISISTNE UP FROM VIAL INTO EQAUSHIELD CLOSED SYSTEM SYRINGE, THE MEDICATION WENT BEHIND THE PLUNGER AND FILLED THE BARREL OF THE SYRINGE. DUE TO THIS, WHEN THE MEDICATION WAS UNABLE TO BE GIVEN AND HAD TO BE WASTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21558853 ↗

Device details

UDI-DI	`07290013484024`
Brand	Equashield
Model	Equashield Syringe Unit
Company	Equashield Medical Ltd
Product code	ONB · Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jul 13, 2023

Device type (GMDN): Medication transfer set

A collection of sterile devices and supplies designed to transfer parenteral medications, and sometimes intravenous (IV) fluids, between a first container(s) [e.g., a vial(s)] and a second container [e.g., an intravenous (IV) bag]; it may also be used to reconstitute medication for its preparation and administration. It is available in a variety of configurations and typically includes tubes, connectors, spike(s), syringes, and caps. This is a single-use device.

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Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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