Medline OR610Recalls & reported problems
Medline Industries, Inc. · TUBING, SUCTION, 1/4" X 10', STRAIGHT · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10888277319189), received between Jan 21, 2025 and Sep 18, 2026 — classified as 1 death, 4 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (3 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
- Loose or Intermittent Connection3
- Connection Problem2
- Decrease in Suction1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Aspiration/Inhalation1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 18, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50820301 ↗MalfunctionSep 15, 2026Connection Problem; Material Deformation
It was reported that "The connector is more rigid and some if the suction tips will not stay connected. The tubing is also very stiff and keeps a memory. This causes issues on the sterile field."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50773195 ↗MalfunctionSep 14, 2026Decrease in Suction; Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50747968 ↗MalfunctionSep 2, 2026Loose or Intermittent Connection
It was reported that the suction tubing they use (OR610) is not consistent in recent lot numbers as they were in the past. The connection is much looser and not practical for every situation it is needed for.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50568252 ↗DeathJan 21, 2025Connection Problem; Connection Problem
ACCORDING TO THE FACILITY ON (B)(6) 2024 THERE WAS A DELAY IN SUCTIONING THE PATIENT AS THE YANKAUER WOULDN'T "PROPERLY CONNECT TO THE SUCTION TUBING".
Patient problems: Aspiration/Inhalation
MAUDE report 21203141 ↗
Other TUBE, ASPIRATING, FLEXIBLE, CONNECTING devices
- DeRoyal 71-C506Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall4 reports
- DeRoyal 71-C512Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall2 reports
- DeRoyal 71-C520Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall1 report
- DeRoyal 71-C6100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C510Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C501Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C5100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C7100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 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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