Mucous Specimen Trap 0035860Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741049293), received between Nov 27, 2019 and Jun 26, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Component Misassembled” (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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 26, 2020Component Misassembled; Device Markings/Labelling Problem; Component Misassembled

  IT WAS REPORTED THAT THE MUCUS TRAP HAD DIFFERENT MARKINGS. IT WAS NOTED THAT ON ONE PRODUCT BELOW THE 10ML, THERE WERE 3 LINES MARKED AND ON ANOTHER PRODUCT, THERE WERE ONLY 2 LINES THAT WERE MARKED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10200046 ↗
• MalfunctionNov 27, 2019Incorrect Measurement; Incorrect Measurement; Fitting Problem

  IT WAS REPORTED THAT THE FITTING THAT ATTACHED THE MUCOUS SPECIMEN TRAP TO THE SUCTION WAS TOO SHORT.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 9386088 ↗