Equashield Luer Lock Adaptor SwivelRecalls & reported problems
Equashield Medical Ltd · Luer Lock Adaptor Swivel · 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 07290013484659), received between Mar 7, 2025 and Mar 7, 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
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 7, 2025
IV CYTARABINE WAS INFUSING. EQUASHIELD CONNECTIONS CHECKED WHEN CHEMO STARTED, ALL WITH TIGHT SEALS. WITH 0.7ML OF CYTARABINE FLUSH LEFT, THIS RN WAS CALLED TO THE ROOM AND SAW DROPS OF BLOOD ON THE BED. PORT LINE THAT HAD CHEMO RUNNING HAD BLOOD BACKED UP THROUGH THE EQUASHEILD AND APPEARED TO BE LEAKING AROUND LEUR LOCK SITE BETWEEN EQUASHIELD AND IV TUBING. RN UNABLE TO DETACH THEM, EQUASHIELD ABLE TO SPIN. PORT LUMEN WAS FLUSHED WITH BRISK BLOOD RETURN. HELD TUBING AS REMAINDER OF CHEMOTHERAPY FLUSH WAS INFUSED WITHOUT ISSUE OR NOTED LEAKING. IV SET UP PLACED IN BAG WITH EQUASHIELD'S AND SET ASIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21547021 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.