YomiLink Teeth Posterior (LRUL) DRW-2081-02Recalls & reported problems
Neocis Inc · YomiLink Teeth Posterior (LRUL) · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810004900608), received between Jun 23, 2026 and Jun 23, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Failure to Disconnect” (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
- Failure to Disconnect1
Patient problems
- Tooth Loss1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 23, 2026Failure to Disconnect
DURING A YOMILINK TEETH (YLT) REMOVAL PROCEDURE, A TOOTH AND A BRIDGE WERE INADVERTENTLY REMOVED. THE PATIENT'S MEDICAL HISTORY INCLUDES EXTENSIVE PRIOR PERIODONTAL WORK. THE PATIENT WAS SUBSEQUENTLY REFERRED TO A GENERAL PRACTITIONER FOR DENTAL TREATMENT. NO FURTHER PATIENT INJURY OR MEDICAL INTERVENTION WAS REPORTED.
Patient problems: Tooth Loss
MAUDE report 25595876 ↗
Other Dental Stereotaxic Instrument devices
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- X-Guide P010673Xnav Technologies LLC · Dental Stereotaxic Instrument1 recall1 report
- X-GUIDE P010701Xnav Technologies LLC · Dental Stereotaxic Instrument1 recall0 reports
- X-GUIDE P010727Xnav Technologies LLC · Dental Stereotaxic Instrument1 recall0 reports
- YomiLink Bone (UL) DRW-1356-01Neocis Inc · Dental Stereotaxic Instrument1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.