Smaxel Fractional CO2 Laser, a Class IV medical laser system.
FDA device recall Z-0804-2025 · posted 2025-01-07 · Open, Classified
Recall details
- Recalling firm
- IDS LTD
- Reason for recall
- The Smaxel Fractional CO2 Laser does not include a Certification label, and adequate instructions for safe operation of the device.
- Action taken
- IDS LTD recommend that users are advised to use it as close to the main body as possible during the procedure. The firm will without charge remedy the defect or bring the product into compliance with each applicable Federal standard. On or about 1/22/2025, the firm mailed a "Notification Letter" to affected customers/users informing them that the SAXEL Fractional CO2 Laser System does not have affixed a certification label and that the firm will be implementing a design change by revising the certification label and will provide the revised certification label free of charge following the design change.
- Root cause
- Radiation Control for Health and Safety Act
- Status
- Open, Classified
- Product code
- ONG
- Quantity affected
- 23
- Distribution
- Worldwide - US Nationwide Distribution
- Date initiated
- 2024-10-16
- Date posted
- 2025-01-07
- Location
- Gwangtan-Myeon
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| SMAXEL CO2 Surgical Laser System (K180036) | Ids, Ltd. | 2018-02-02 |