MEDLINE INDUSTRIES, INC. OR212Recalls & reported problems
Medline Industries, Inc. · CANISTER, RIGID, 1200CC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 40888277363343), received between Nov 6, 2024 and Sep 30, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Break” (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. 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
- Break2
- Crack2
- Suction Problem2
- Burst Container or Vessel1
- Component Missing1
- Infusion or Flow Problem1
- Loose or Intermittent Connection1
- Material Discolored1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
- Choking1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Physical Resistance/Sticking
It was reported that "The lids are stuck on the canister itself and we are unable to remove it safely with out breaking the canister. These usually come in separated but for these they are already put together."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50945501 ↗MalfunctionSep 28, 2026Material Discolored; Infusion or Flow Problem
It was reported that "DISCOLORED CYLINDER. THE CUSTOMER HAS SEVERAL REPORTS OF THESE CYLINDERS NOT WORKING CORRECTLY DUE TO WHAT THE ASSOCIATES THINK IS A CHECK VALVE ISSUE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918866 ↗MalfunctionSep 18, 2026Suction Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50828725 ↗MalfunctionSep 15, 2026Break; Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50772069 ↗MalfunctionSep 13, 2026Component Missing
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50747558 ↗MalfunctionSep 8, 2026Burst Container or Vessel; Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50673185 ↗MalfunctionSep 8, 2026Break
It was reported that THIS ITEM WAS DAMAGED AND BROKEN IN HALF WHEN SHE RECEIVED IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50670861 ↗MalfunctionSep 2, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50569401 ↗MalfunctionNov 6, 2024Suction Problem; Suction Problem
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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