Rube 24621Recalls & reported problems
Medtronic Xomed, Inc. · VENT TUBE 24621 5PK RUBE T GROM 1.14 SIL · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00681490062800), received between Mar 28, 2025 and Feb 17, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (1 report).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
- Loss of Osseointegration1
Patient problems
- Failure of Implant2
- Inflammation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 17, 2026Fracture
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FRACTURE. A PIECE HAD BROKEN OFF THE IMPLANT COLLAR.
Patient problems: Failure of Implant
MAUDE report 24364146 ↗InjuryMar 28, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Inflammation
MAUDE report 21719097 ↗
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- NeoZoline NZ3309Adept Medical Limited · Tube, Tympanostomy1 recall0 reports
- NeoZoline NZ3309-2Adept Medical Limited · Tube, Tympanostomy1 recall0 reports
- NeoZoline NZ3306-2Adept Medical Limited · Tube, Tympanostomy1 recall0 reports
- NeoZoline NZ3306Adept Medical Limited · Tube, Tympanostomy1 recall0 reports
- Gyrus ACMI 240044Gyrus ACMI, LLC · TUBE, TYMPANOSTOMY1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.