MEDLINE INDUSTRIES, INC. OR220Recalls & reported problems
Medline Industries, Inc. · CANISTER, RIGID, 2000CC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 40888277363350), received between Mar 27, 2025 and Sep 22, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Component Missing” (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
- Component Missing1
- Suction Failure1
- Suction Problem1
Patient problems
- Aspiration/Inhalation1
- Exposure to Body Fluids1
- Hypoxia1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Component Missing
It was reported that "cant run, 1ea scuffed/cracked, 4ea missing elbow" and "we are missing 4 of the elbows for the lids."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50855675 ↗MalfunctionSep 8, 2026Suction Problem
It was reported that the RN noticed that it stopped suctioning urine. Andrew, an ICU CNA, noticed that it would suction a little bit if he disconnected then reconnected suctioning, but then would stop again.
Patient problems: Exposure to Body Fluids
MAUDE report 50668589 ↗InjuryMar 27, 2025Suction Failure; Suction Failure
ACCORDING TO THE CUSTOMER, ON (B)(6)2025 WHEN ATTEMPTING TO SUCTION THE PATIENT'S VOMIT DURING INTUBATION, THEY WERE "UNABLE TO SUCTION EMESIS", THE PATIENT ASPIRATED, AND "DEVELOPED SEVERE HYPOXEMIA FOLLOWED BY PEA ARREST".
Patient problems: Aspiration/Inhalation; Hypoxia
MAUDE report 21712460 ↗
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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