MAHURKAR 8830414001Recalls & reported problems
Mozarc Medical US LLC · Acute Dual Lumen Catheter,Straight Extensions with 2 Sealing Caps · Class 2
All models of MAHURKAR (81)
Data updated Oct 18, 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 10884521005129), received between Mar 30, 2020 and Mar 30, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Product Quality Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Product Quality Problem1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 30, 2020Product Quality Problem; Product Quality Problem
ACCORDING TO THE REPORTER, POST OPERATIVELY, AFTER INSERTING THE CATHETER VIA RIGHT JUGULAR POSITION, IT WAS STATED THAT IT WAS SECURED IN PLACE BY BINDING IT TO A PLASTIC RING INSERTED/SECURED IN THE PATIENT SKIN, 2 DAYS AFTER, IT WAS NOTED THAT THE CATHETER SLIPPED OUT OF PLACE WITHOUT ANY EXTERNAL FORCE APPLIED. DUE TO THE SLIPPING, THE CATHETER WAS REMOVED. THERE WAS NO REPORTED PATIENT CONSEQUENCE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9899684 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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