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DeRoyal NP-1140-USRecalls & reported problems

Deroyal Industries, Inc. · Canister 140ml - Prospera(R) Mini · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00749756934787), received between Nov 27, 2018 and Nov 27, 2018 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Component Misassembled” (3 reports).

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.

Most reported problems

Device problems

  • Component Misassembled3
  • Manufacturing, Packaging or Shipping Problem3

Patient problems

  • No Consequences Or Impact To Patient2
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 27, 2018Manufacturing, Packaging or Shipping Problem; Component Misassembled; Manufacturing, Packaging or Shipping Problem; Component Misassembled

    A NEGATIVE PRESSURE WOUND THERAPY PUMP WOULD REGISTER A "FULL CANISTER ALARM" EVEN WHEN THE CANISTER WAS NOT FULL. IN THIS INSTANCE, THERE WAS NO PATIENT EFFECT, BUT THE POTENTIAL FOR DISRUPTION TO THERAPY MAY EXIST IN THE FUTURE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8109282 ↗
  • MalfunctionNov 27, 2018Manufacturing, Packaging or Shipping Problem; Component Misassembled; Manufacturing, Packaging or Shipping Problem; Component Misassembled

    A NEGATIVE PRESSURE WOUND THERAPY PUMP WOULD REGISTER A "FULL CANISTER ALARM" EVEN WHEN THE CANISTER WAS NOT FULL. IN THIS INSTANCE, THERE WAS NO PATIENT EFFECT, BUT THE POTENTIAL FOR DISRUPTION TO THERAPY MAY EXIST IN THE FUTURE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8109281 ↗
  • MalfunctionNov 27, 2018Manufacturing, Packaging or Shipping Problem; Component Misassembled; Manufacturing, Packaging or Shipping Problem; Component Misassembled

    A NEGATIVE PRESSURE WOUND THERAPY PUMP WOULD REGISTER A "FULL CANISTER ALARM" EVEN WHEN THE CANISTER WAS NOT FULL. IN THIS INSTANCE, THERE WAS NO PATIENT EFFECT, BUT THE POTENTIAL FOR DISRUPTION TO THERAPY MAY EXIST IN THE FUTURE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8109279 ↗

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Sources and updates

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