MEDLINE INDUSTRIES, INC. OR230Recalls & reported problems
Medline Industries, Inc. · CANISTER, RIGID, 3000CC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 40888277363367), received between May 21, 2026 and Sep 21, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Crack” (6 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
- Crack6
- Explosion5
- Fluid/Blood Leak3
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Crack; Explosion
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50846203 ↗MalfunctionSep 18, 2026Crack; Explosion
It was reported that "4 cracked suction canisters and 1 suction canister actually exploded all over the operating room."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50819844 ↗MalfunctionSep 15, 2026Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778752 ↗MalfunctionSep 10, 2026Crack; Fluid/Blood Leak; Explosion
It was reported that "4 cracked suction canisters and 1 suction canister actually exploded all over the OR."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50714297 ↗MalfunctionSep 8, 2026Crack; Fluid/Blood Leak; Explosion
It was reported that "4 cracked suction canisters and 1 suction canister actually exploded all over the operating room."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50675487 ↗MalfunctionSep 7, 2026Crack; Fluid/Blood Leak; Explosion
It was reported that 4 cracked suction canisters and 1 suction canister actually exploded all over the OR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50652310 ↗MalfunctionMay 21, 2026Break
PER EMAIL CUSTOMER STATES CANISTER EXPLODED WHILE CONNECTED TO SUCTION REGULATOR, WAS CONNECTED BUT PATIENT WAS NOT USING THE YANKAUER AT THE TIME OF THIS EVENT. CANISTER SHATTERED INTO SEVERAL PIECES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25249365 ↗
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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