Medline DYNDSCL1500Recalls & reported problems
Medline Industries, Inc. · LINER,SOFT,SUCTION CANISTER,1500CC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 10884389129531), received between Oct 26, 2023 and Sep 22, 2026 — classified as 2 injuries, 10 malfunctions.
The most frequently reported specific device problem is “Suction Failure” (4 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Mar 22, 2024Class IIOpen, Classified
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Z-2694-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Suction Failure4
- Suction Problem4
- Decrease in Suction1
- Difficult to Open or Close1
- Fluid/Blood Leak1
- Mechanical Problem1
- Nonstandard Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions11
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Aspiration/Inhalation1
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Difficult to Open or Close
It was reported that "ITEM WASN'T WORKING. THEY WEREN'T CLOSING".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50855189 ↗MalfunctionSep 10, 2026Suction Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50717380 ↗MalfunctionSep 10, 2026Suction Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50715766 ↗MalfunctionSep 9, 2026Suction Problem
It was reported that ¿The vacuum does not work on many 1.5L liners. As soon as the 1.5L suction liners are put in place, they suck little or nothing. Varies by lot.¿
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50690924 ↗MalfunctionSep 8, 2026Decrease in Suction
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50675754 ↗MalfunctionSep 8, 2026Suction Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50672521 ↗MalfunctionSep 2, 2026Suction Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50572931 ↗MalfunctionSep 2, 2026Nonstandard Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50570191 ↗MalfunctionSep 2, 2026Fluid/Blood Leak
It was reported that "leaking".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50567789 ↗MalfunctionSep 2, 2026Suction Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50564674 ↗OtherSep 1, 2026Suction Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50542561 ↗InjuryDec 20, 2023Suction Failure; Suction Failure
ACCORDING TO THE CUSTOMER, DURING THE CARDIAC ARREST OF A PATIENT ON (B)(6) 2023 THE SUCTION "STOPPED" FUNCTIONING AT THE BEGINNING OF TREATMENT BUT, THEN BEGAN FUNCTIONING "WEAKLY".
Patient problems: Aspiration/Inhalation
MAUDE report 18370275 ↗InjuryOct 26, 2023Mechanical Problem; Mechanical Problem
ACCORDING TO THE CUSTOMER, THE SUCTION LINER "REPEATEDLY" HAD LITTLE OR NO SUCTION CAUSING A PATIENT TO BE "REANIMATED" AS A RESULT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 18015247 ↗
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
- PNEUMOSTAT 16100Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall3 deaths12 reports
- OCEAN 2002-300Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall10 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 · each recall links to the FDA recall notice
- 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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