Medline DYNDCLO1500Recalls & reported problems
Medline Industries, Inc. · OUTER CANISTER, SOFT LINER, 1500CC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 2
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10884389129593), received between Apr 21, 2023 and Sep 14, 2026 — classified as 2 deaths, 2 malfunctions.
The most frequently reported specific device problem is “Crack” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Crack1
- Detachment of Device or Device Component1
- Material Integrity Problem1
- Suction Problem1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Aspiration/Inhalation1
- Cardiac Arrest1
- Respiratory Arrest1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 14, 2026Crack
It was reported that "Rigid Outer Canniser -cracked or chipped."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50754171 ↗OtherSep 11, 2026Material Integrity Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50732865 ↗MalfunctionSep 8, 2026Detachment of Device or Device Component
It was reported that "The bottom of the canister looks to be glued instead of being manufactured as one solid piece, which during the reserialization process in the CSSD the canister bottom was detached."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50674703 ↗DeathJan 29, 2025Use of Device Problem; Use of Device Problem
IT WAS REPORTED BY THE USER FACILITY THAT DURING A MEDICAL EMERGENCY, SUCTION OF THE AIRWAY WAS REQUIRED IN ORDER TO INTUBATE THE PATIENT, HOWEVER THE WALLED SUCTION UNIT WAS NOT SET UP READY TO USE AND WHEN SET UP, IT DID NOT WORK CORRECTLY.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 21266850 ↗DeathApr 21, 2023Suction Problem; Suction Problem
IT WAS REPORTED THAT THERE WAS NO SUCTION FROM THE DEVICE.
Patient problems: Aspiration/Inhalation; Cardiac Arrest; Respiratory Arrest
MAUDE report 16786141 ↗
Other BOTTLE, COLLECTION, VACUUM devices
- OASIS 3600-100Atrium Medical Corporation · Bottle, Collection, Vacuum3 recalls1 death175 reports
- OCEAN 2002-000Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM3 recalls44 reports
- EXPRESS 16400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall110 reports
- EXPRESS 4000-100NAtrium Medical Corporation · Bottle, Collection, Vacuum2 recalls30 reports
- OCEAN 2002-400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM2 recalls18 reports
- OASIS 3612-100Atrium Medical Corporation · Bottle, Collection, Vacuum1 recall18 reports
- Medline DYNDSCL1500Medline Industries, Inc. · BOTTLE, COLLECTION, VACUUM1 recall13 reports
- PNEUMOSTAT 16100Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall3 deaths12 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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