Medline DYND50130Recalls & reported problems
Medline Industries, Inc. · YANKAUER,BULB TIP,W/O VENT,RIGID,STERILE · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10080196034956), received between Mar 23, 2023 and Sep 16, 2026 — classified as 2 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Material Integrity Problem” (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
- Material Integrity Problem3
- Crack1
- Gas/Air Leak1
- Material Puncture/Hole1
- Material Split, Cut or Torn1
Patient problems
- Foreign Body In Patient1
- Hemorrhage/Blood Loss/Bleeding1
- Insufficient Information1
- Laceration(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Material Split, Cut or Torn
It was reported that ¿(b)(6) Hospital # (b)(6) received in product for item # DYND50130 and has a slit in the tubing and is not able to use.¿
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50787560 ↗InjuryNov 4, 2025Crack; Material Integrity Problem; Crack; Material Integrity Problem
ACCORDING TO THE FACILITY, DURING AN ENT CASE, "THERE WAS A SMALL CRACK ON THE TOP OF THE SUCTION TIP THAT WAS NOT RECOGNIZED BY THE SURGICAL TEAM. THE SURGEON USED THE SUCTION TIP IN THE THROAT AND THE CRACK IN THE SUCTION TIP CAUGHT THE UVULA AND CAUSED A SMALL TEAR IN THE UVULA. THE SURGEON WAS ABLE TO CAUTERIZE WITHOUT FURTHER ISSUE."
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 23467281 ↗MalfunctionJan 2, 2025Material Integrity Problem; Material Integrity Problem
InjuryJun 4, 2024Material Integrity Problem; Material Integrity Problem
ACCORDING TO THE FACILITY (B)(6) 2024 "SUCTION WAS USED TO SUCTION ANY ORAL SECRETIONS WITH THE TIP OF THE SUCTION, HAD BEEN OFF AND DURING THE SUCTION AND CAUSED A LACERATION OF THE RIGHT PALATE".
Patient problems: Laceration(s)
MAUDE report 19458911 ↗MalfunctionMar 23, 2023Material Puncture/Hole; Gas/Air Leak
YANKAUER SUCTION VENT, HOLE IN THE HANDLE THAT LEAKING AIR, NOT FUNCTIONING WELL WHEN SUCTION. THE DEVICE SUCKS THROUGH SIDE NOT TIP.
Patient problems: Insufficient Information
MAUDE report 16610657 ↗
Other CATHETER AND TIP, SUCTION devices
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- Wayne G56537Cook Incorporated · CATHETER AND TIP, SUCTION2 recalls33 reports
- Bard® Suction Connector EN0066000C. R. Bard, Inc. · CATHETER AND TIP, SUCTION1 recall6 reports
- CLEARVIEW® 31200Medtronic, Inc. · CATHETER AND TIP, SUCTION1 recall0 reports
- ARROW IPN039282Teleflex Incorporated · CATHETER AND TIP, SUCTION1 recall0 reports
- ARROW IPN037088Teleflex Incorporated · CATHETER AND TIP, SUCTION1 recall0 reports
- ARROW IPN922898Teleflex Incorporated · CATHETER AND TIP, SUCTION1 recall0 reports
- Medline Industries, Inc. OR929KMedline Industries, Inc. · CATHETER AND TIP, SUCTION1 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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