ParaPost Fiber Lux PF1714Recalls & reported problems
Coltene/Whaledent Inc · 5 ParaPost FiberLux Posts, Size 4 · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 D661PF17141), received between Nov 21, 2025 and Nov 21, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Burning Sensation1
- Discomfort1
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 21, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
ON (B)(6), COLTENE RECIEVED A REPORT FROM A PATIENT EXPALINING THAT AFTER 2 1/2 YEARS OF A BURNING SENSATION, SHE VOLUNTARILY HAD A DENTAL IMPLANT USING COLTENE'S POST ALONG WITH ANOTHER MANUFACTURER'S POST AND CORE MATERIAL REMOVED DUE TO AN ALLERGIC REACTION. THE PATIENT SAID SHE HAD EXTENSIVE ALLERGY TESTING, WHICH LED TO A DOUBLE POSITIVE REACTION TO TITANIUM DIOXIDE AND WAS INQUIRING WHETHER OR NOT COLTENE'S PRODUCT NUMBER PF1714 CONTAINED TITANIUM DIOXIDE. NO BATCH NUMBER WAS GIVEN NOR AVAILABLE. ADDITIONAL INFORMATION FOR OTHER COMPOUNDS USED IN THE PATIENT'S PROCEDURE WAS ATTEMPTED BUT NOT RECEIVED. COLTENE PRODUCT NUMBER PF1714 DOES NOT CONTAIN TITANIUM DIOXIDE.
Patient problems: Burning Sensation; Discomfort; Insufficient Information
MAUDE report 23617222 ↗
Other Post, Root Canal devices
- ParaPost XT P6850Coltene/Whaledent Inc · Post, Root Canal1 report
- GT Post and Drills GTPOSTF1Tulsa Dental Products LLC · POST, ROOT CANAL1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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