AH Plus BioCermanic SealerRecalls & reported problems across all models
Tulsa Dental Products LLC · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 56
- Deaths reported
- 0
- Injuries reported
- 30
- Recalls
- 0
We found 2 models of AH Plus BioCermanic Sealer by Tulsa Dental Products LLC in the FDA's device registry (GUDID). Together they are named in 56 adverse event reports in the FDA's MAUDE database, received between Jan 16, 2025 and Mar 3, 2026 — classified as 30 injuries, 26 malfunctions.
The most frequently reported specific device problem is “Material Erosion” (43 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported AH Plus BioCermanic Sealer problems
Device problems
- Material Erosion43
- Lack of Effect10
- Short Fill3
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available43
- No Clinical Signs, Symptoms or Conditions13
AH Plus BioCermanic Sealer models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- AH Plus BioCermanic Sealer AHPBIOSEALRESIN, ROOT CANAL FILLING46 reports
- AH Plus BioCermanic Sealer AHPBIOREFILLRESIN, ROOT CANAL FILLING10 reports
Recent AH Plus BioCermanic Sealer adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionMar 3, 2026Material Erosion
IN THIS EVENT IT IS REPORTED THAT WHEN USING THE AH PLUS BIOCERAMIC SEALER STARTER KIT SOME PATIENTS RETURNED AND REQUIRED RETREATMENT DUE TO THE RESORPTION OF THE SEALER.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 24498513 ↗MalfunctionMar 3, 2026Material Erosion
IN THIS EVENT IT IS REPORTED THAT WHEN USING THE AH PLUS BIOCERAMIC SEALER STARTER KIT SOME PATIENTS RETURNED AND REQUIRED RETREATMENT DUE TO THE RESORPTION OF THE SEALER.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 24498429 ↗MalfunctionMar 3, 2026Material Erosion
IN THIS EVENT IT IS REPORTED THAT WHEN USING THE AH PLUS BIOCERAMIC SEALER STARTER KIT SOME PATIENTS RETURNED AND REQUIRED RETREATMENT DUE TO THE RESORPTION OF THE SEALER.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 24498382 ↗MalfunctionMar 3, 2026Material Erosion
IN THIS EVENT, IT IS REPORTED THAT WHEN USING THE AH PLUS BIOCERAMIC SEALER STARTER KIT, SOME PATIENTS RETURNED AND REQUIRED RETREATMENT DUE TO THE RESORPTION OF THE SEALER.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 24498284 ↗MalfunctionFeb 12, 2026Short Fill
IN THIS EVENT IT IS REPORTED THAT AFTER USE OF AH PLUS BIOCERAMIC SEALER SOME PATIENTS RETURNED WITH NO SEALER, NO FILL OR HAD SHORT FILLS. PATIENT REQUIRED RETREATMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24321333 ↗MalfunctionFeb 4, 2026Short Fill
IN THIS EVENT IT IS REPORTED THAT AHPBIOSEAL- AH PLUS BIOCERAMIC SEALER STARTER KIT - THAT WAS USED IN TREATMENT IT WAS FOUND AFTER THE PATIENT RETURNED THERE WAS NO SEALER AND THERE WERE SHORT FILLS. PATIENT WAS RETREATED. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24257879 ↗MalfunctionFeb 4, 2026Short Fill
IN THIS EVENT IT IS REPORTED THAT AHPBIOSEAL- AH PLUS BIOCERAMIC SEALER STARTER KIT - THAT WAS USED IN TREATMENT IT WAS FOUND AFTER THE PATIENT RETURNED THERE WAS NO SEALER AND THERE WERE SHORT FILLS. PATIENT WAS RETREATED. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24257768 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769658 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769645 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769636 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769612 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769606 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769599 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769421 ↗InjuryAug 11, 2025Lack of Effect; Lack of Effect
IN THIS EVENT IT WAS REPORTED THAT THE AHPBIOSEAL SHOWED RESORPTION REQUIRING RETREATMENT. NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22769404 ↗
Other Tulsa Dental Products LLC products
All Tulsa Dental Products LLC devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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