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SSCOR Duet ® 2314NBRecalls & reported problems

Sscor, Inc. · Portable Suction Device · 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 B2452314NB0), received between Sep 15, 2023 and Sep 15, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Battery 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Battery Problem1

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.

  • MalfunctionSep 15, 2023Battery Problem; Battery Problem

    A SCORT SUCTION UNIT (WITH NEW BATTERIES INSTALLED IN (B)(6) 2022 AND REPLACE BATTERY INDICATOR OFF) FAILED WHEN USED ON A PATIENT DURING A CRASH.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17761283 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.