Split Cath® III ASPC40-3Recalls & reported problems
Medical Components, Inc. · 14F X 40CM SPLIT CATH® III CATHETER SET (CUFF 35CM FROM TIP) · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884908004205), received between Sep 22, 2017 and Sep 22, 2017 — classified as 1 death.
The most frequently reported specific device problem is “Failure to Advance” (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
- Failure to Advance1
- Physical Resistance1
Patient problems
- Death1
- Erythema1
- Exsanguination1
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathSep 22, 2017Failure to Advance; Physical Resistance; Failure to Advance; Physical Resistance
PERFORATION DURING CATHETER EXCHANGE.
Patient problems: Death; Erythema; Exsanguination; Perforation
MAUDE report 6887920 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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