Medline HCS7850Recalls & reported problems
Medline Industries, Inc. · CANISTER,SUCTION,850 CC W/FLOAT LID · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 23
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 23 adverse event reports that list this exact device (DI 40884389144566), received between Jan 14, 2026 and Sep 30, 2026 — classified as 3 injuries, 20 malfunctions.
The most frequently reported specific device problem is “Suction Problem” (7 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Suction Problem7
- Crack5
- Fitting Problem5
- Break3
- Material Deformation3
- Component Missing1
- Decrease in Suction1
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions20
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available3
Recent adverse event reports
The 23 most recent of 23 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fitting Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950061 ↗MalfunctionSep 22, 2026Suction Problem
It was reported that "THE SUCTION STOPPED WORKING. THE HOSE FROM HER TRACH ISN'T WORKING".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854805 ↗MalfunctionSep 18, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50829494 ↗MalfunctionSep 17, 2026Suction Problem
It was reported that "NOT WORKING PROPERLY ; NOT SUCTIONING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50806080 ↗MalfunctionSep 16, 2026Component Missing
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794941 ↗MalfunctionSep 13, 2026Crack; Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50746898 ↗MalfunctionSep 11, 2026Fitting Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50736207 ↗MalfunctionSep 10, 2026Decrease in Suction
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50717027 ↗MalfunctionSep 8, 2026Break; Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50679392 ↗MalfunctionSep 8, 2026Fitting Problem; Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50673587 ↗MalfunctionSep 8, 2026Crack
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50671909 ↗MalfunctionSep 1, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50551250 ↗MalfunctionAug 28, 2026Fitting Problem; Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50501089 ↗MalfunctionAug 26, 2026Suction Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50459060 ↗MalfunctionAug 25, 2026Crack; Material Fragmentation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50433765 ↗MalfunctionAug 25, 2026Suction Problem; Obstruction of Flow
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50432886 ↗MalfunctionAug 25, 2026Suction Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50430656 ↗MalfunctionAug 20, 2026Crack
It was reported that "PER CST, HE JUST OPENED UNDAMAGED BOX AND NOTICED A CRACKED CANISTER".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50346589 ↗MalfunctionAug 18, 2026Fracture; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50300484 ↗MalfunctionAug 17, 2026Fitting Problem
It was reported that she has to poke a hole in the canister/lid in order for the suction to work.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50275596 ↗InjuryJan 15, 2026Suction Problem
ACCORDING TO THE FACILITY, A RESIDENT WAS IN NEED OF EMERGENCY SUCTION. DURING THE EVENT, A TOTAL OF THREE CANISTERS WERE REPORTEDLY OBTAINED AND ALL THREE DID NOT PROVIDE SUCTION. THE RESIDENT WAS SENT TO THE ER AND ADMITTED TO THE HOSPITAL. THE FACILITY STATED THE RESIDENT PASSED AWAY BUT THAT THE CAUSE OF DEATH WAS NOT BECAUSE OF THE CANISTERS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 24082687 ↗InjuryJan 15, 2026Suction Problem
ACCORDING TO THE FACILITY, A RESIDENT WAS IN NEED OF EMERGENCY SUCTION. DURING THE EVENT, A TOTAL OF THREE CANISTERS WERE REPORTEDLY OBTAINED AND ALL THREE DID NOT PROVIDE SUCTION. THE RESIDENT WAS SENT TO THE ER AND ADMITTED TO THE HOSPITAL. THE FACILITY STATED THE RESIDENT PASSED AWAY BUT THAT THE CAUSE OF DEATH WAS NOT BECAUSE OF THE CANISTERS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 24081939 ↗InjuryJan 14, 2026Suction Problem
ACCORDING TO THE FACILITY, A RESIDENT WAS IN NEED OF EMERGENCY SUCTION. DURING THE EVENT, A TOTAL OF THREE CANISTERS WERE REPORTEDLY OBTAINED AND ALL THREE DID NOT PROVIDE SUCTION. THE RESIDENT WAS SENT TO THE ER AND ADMITTED TO THE HOSPITAL. THE FACILITY STATED THE RESIDENT PASSED AWAY BUT THAT THE CAUSE OF DEATH WAS NOT BECAUSE OF THE CANISTERS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 24075000 ↗
Other BOTTLE, COLLECTION, VACUUM devices
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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