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DeRoyal 71-8002Recalls & reported problems

Deroyal Industries, Inc. · ECO Rigid Canister 1200cc1200cc w/2 elbows · 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 00749756375788), received between Aug 9, 2024 and Aug 9, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Suction Problem” (2 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 2 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Suction Problem2

Patient problems

  • Insufficient Information2

Recent adverse event reports

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

  • MalfunctionAug 9, 2024Suction Problem; Suction Problem

    A USER FACILITY REPORTED, " WE HAD CANISTER THAT DID WORK ON 3 NORTH THE NEXT DAY IN WHICH THE LID CAME OFF OF THE CANISTER WHILE NURSING WAS SUCTIONING A PATIENT THAT WAS HAVING A SEIZURE. THIS PRODUCT IS FREQUENTLY NEEDED IN EMERGENCY SITUATIONS AND IT IS WITH A EXTREMELY IMPORTANT THAT THIS PRODUCT WORKS WITHOUT FAIL EVERY SINGLE TIME. IN AN EMERGENCY SITUATION THERE IS NOT TIME TO FIDDLE AROUND SUCTION CANISTER TO FIGURE OUT WHAT IS GOING WRONG, SUCTION IS ALWAYS AN URGENT NEED."

    Patient problems: Insufficient Information

    MAUDE report 19950650 ↗
  • MalfunctionAug 9, 2024Suction Problem; Suction Problem

    A USER FACILITY REPORTED, " THESE SUCTION CANISTERS ARE NOT SUCTIONING PROPERLY, ON 3 WEST WE HAD AN URGENT SITUATION IN WHICH A TRACH PATIENT NEEDED SUCTIONED AND WE WENT THROUGH 3 DIFFERENT SUCTION CANISTERS AND NONE OF THEM WERE SUCTIONING PROPERLY, THEY ALL HAD VERY LITTLE SUCTION COMING OUT OF THEM EVEN THOUGH THE SUCTION REGULATOR WAS TURNED ALL THE WAY UP. THE LID WAS ON CORRECTLY, THE SUCTION WAS SET UP PROPERLY, THERE WAS JUST NOT ENOUGH SUCTION. WE HAD TO OPEN THE CRASH CART JUST TO GET ONE OF THE OLD CANISTERS (WITH A WHITE LID) THAT WE USED BEFORE THIS ONE, AND THANKFULLY WE ALSO HAD ANOTHER THAT DID WORK. THIS PRODUCT IS FREQUENTLY NEEDED IN EMERGENCY SITUATIONS AND IT IS WITH A EXTREMELY IMPORTANT THAT THIS PRODUCT WORKS WITHOUT FAIL EVERY SINGLE TIME. IN AN EMERGENCY SITUATION THERE IS NOT TIME TO FIDDLE AROUND SUCTION CANISTER TO FIGURE OUT WHAT IS GOING WRONG, SUCTION IS ALWAYS AN URGENT NEED."

    Patient problems: Insufficient Information

    MAUDE report 19950644 ↗

Other BOTTLE, COLLECTION, VACUUM devices

All BOTTLE, COLLECTION, VACUUM devices →

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