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SOLTIVE TFL-AFS 365Recalls & reported problems

Gyrus ACMI, LLC · TFL FIBER STRIPPER, 365 MICRON, AUTOCLAVABLE · Class 2

All models of SOLTIVE (16)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00821925044401), received between Sep 30, 2022 and Sep 30, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

7 other recalls cover devices cleared under the same FDA submission (K242191); they may or may not involve this specific model.

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.

Most reported problems

Device problems

  • Break1
  • Output Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2022Break; Output Problem; Break; Output Problem

    CUSTOMER SALES REPRESENTATIVE REPORTED DURING AN UNSPECIFIED PROCEDURE, AS THE USERS WERE FIRING THE LASER, THE FIBER CONNECTION TO THE PLASTIC PIECE CAME OFF AND THE LASER KEPT ON FIRING EVEN THOUGH THE USERS WERE NOT FIRING. THE LASER DID NOT STOP UNTIL THE USERS UNPLUGGED THE FIBER. ACCORDING TO THE REPORTER, THE LASER ITSELF WAS WORKING, CUSTOMER TRIED A NEW FIBER AND WORKED WITHOUT ANY ISSUES. THERE WAS NO PATIENT HARM, NO USER INJURY REPORTED DUE TO THE EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15516126 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K242191. One submission often covers many models, so check the product and lot details in each record.

  • Z-1694-2026 · Feb 27, 2026 · Open, Classified
    Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-CPLU Product Descriptio
  • Z-1695-2026 · Feb 27, 2026 · Open, Classified
    Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An el
  • Z-1923-2025 · May 6, 2025 · Open, Classified
    Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable Laser Fibers Model/Catalog Number: TFL-FBX150R, TFL-FBX200R, TFL-FBX365R, TFL-FBX550R, TFL-FBX940R, TFL
  • Z-1920-2025 · May 6, 2025 · Open, Classified
    Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Number: TFL-SLS, TFL-SLS-JA (Japan only); Product Description: SOLTIV
  • Z-1922-2025 · May 6, 2025 · Open, Classified
    Brand Name: Powered Laser Surgical Instrument Product Name: Soltive SuperPulsed Laser Fibers - Single Use Model/Catalog Numbers: TFL-FBX150BS, TFL-FBX200BS, TFL-FBX150S, TFL-FBX200
  • Z-1921-2025 · May 6, 2025 · Open, Classified
    Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A P
  • Z-1715-2025 · Apr 4, 2025 · Open, Classified
    Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Numbers: TFL-SLS, TFL-PLS Product Description: SOLTIVE Laser Systems

Other Powered laser surgical instrument devices

All Powered laser surgical instrument devices →

Sources and updates

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