Recall archive / FDA device enforcement
SOLTIVE SuperPulsed Laser Fibers, Model No. TFL-FBX200BS — FDA record Z-0718-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 4, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- SOLTIVE SuperPulsed Laser Fibers, Model No. TFL-FBX200BS
- Reason
- Affected products may potentially have a breached sterile pouch seal. A breached sterile pouch seal may lead to minor procedure delays (if noticed prior to use) or patient infections (if not noticed prior to use in patient).
- Classification
- Class II
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 179 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0718-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI 00821925043985 Lot KR262848 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Domestic distribution to the following states: AK AR AZ CA FL GA IA ID IN KS KY LA MA MI NC ND NE NJ NY OR PA SC SD TN TX VA WI International distribution to Canada, Latin America, and Europe.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jan 24, 2024
- Recall initiation date
- Dec 4, 2023
- Center classification date
- Jan 12, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.