SSCOR DUET 2314Recalls & reported problems
Sscor, Inc. · Portable Suction Device · Class 2
Data updated Oct 16, 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 B24523140), received between May 9, 2024 and May 9, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Run on Battery” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Run on Battery1
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.
MalfunctionMay 9, 2024Failure to Run on Battery; Failure to Run on Battery
2314 FAILED TO OPERATE ON BATTERY POWER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19281296 ↗
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- CARE-E-VAC 3Ohio Medical, LLC · Pump, Portable, Aspiration (Manual Or Powered)8 reports
- Thopaz+Medela AG · Pump, Portable, Aspiration (Manual Or Powered)2 reports
- SSCOR Duet ® 2314NBSscor, Inc. · Pump, Portable, Aspiration (Manual Or Powered)1 report
- Thopaz+Medela AG · Pump, Portable, Aspiration (Manual Or Powered)1 death1 report
- Aspirator 798-0330-01Zoll Medical Corporation · PUMP, PORTABLE, ASPIRATION (MANUAL OR POWERED)1 report
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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