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Open, Classified

Smaxel Fractional CO2 Laser, a Class IV medical laser system.

FDA Recall Z-0804-2025 · Posted 2025-01-07

Recalling FirmIDS LTD
Recall StatusOpen, Classified
Product CodeONG
Date Initiated2024-10-16
Product Quantity23

Reason for Recall

The Smaxel Fractional CO2 Laser does not include a Certification label, and adequate instructions for safe operation of the device.

Firm Action

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

Distribution Pattern

Worldwide - US Nationwide Distribution

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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