Compat Enteral Feeding tube 12Fr 120cm with stylet N560Recalls & reported problems
Cedic Srl · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08056093720976), received between Jan 2, 2020 and Mar 1, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Displays Incorrect Message” (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
- Device Displays Incorrect Message1
- Noise, Audible1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Patient Involvement1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 1, 2022Noise, Audible; Noise, Audible
ACCORDING TO THE REPORTER, DURING SERVICE AND REPAIR, THE UNIT SPEAKER WAS DEFECTIVE. IT WAS STATED THAT WHEN THE UNIT WAS TURNED ON THERE WAS NO SOUND AND FOUND THAT ONE OF THE CABLES WERE BROKEN. THE SPEAKER WAS REPLACED WITH A NEW ONE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13626809 ↗MalfunctionJan 2, 2020Device Displays Incorrect Message; Device Displays Incorrect Message
ACCORDING TO THE REPORTER, THE UNIT HAD DISPLAY FAILURE. THE CUSTOMER ALSO STATED THERE WAS MISSING SEGMENTS EVERY DIGIT. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 9538087 ↗
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- EndoVive Standard PEG Kit M00509050Boston Scientific Corporation · Gastrointestinal Tubes with Enteral Specific Connectors1 recall6 reports
- Salem Sump 8888264986ECardinal Health 200, LLC · Gastrointestinal Tubes with Enteral Specific Connectors1 recall1 death2 reports
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- Salem Sump 7771610ECardinal Health, Inc. · Gastrointestinal Tubes with Enteral Specific Connectors1 death18 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.