IDS LTD recalls Smax:el Fractional CO2 Laser devices lacking certification labels and safety instructions. Consumers should check for missing labels and contact the company for details.
The Smaxel Fractional CO2 Laser does not include a Certification label, and adequate instructions for safe operation of the device.
IDS LTD is recalling Smaxel Fractional CO2 Laser devices because they lack required certification labels and safety instructions. This could lead to improper use and potential injury if the device is operated without proper guidance.
The device lacks a certification label and adequate safety instructions, which are critical for proper operation. Without these, users may operate the laser incorrectly, potentially causing injury. However, the hazard does not involve immediate risks like fire or death in normal use.
Users of the Smaxel Fractional CO2 Laser devices who purchased them from unknown sources or retailers that did not verify the product's certification. Medical professionals using the device without proper instructions are at higher risk.
Check for the absence of a certification label and safety instructions on the device. The product was sold under unknown conditions, so it's unclear which retailers or dates are affected.
Look for a certification label on the device; if missing, the product is part of the recall.
The Smaxel Fractional CO2 Laser lacks a certification label and adequate safety instructions, which are required for proper operation.
Check for the absence of a certification label and safety instructions on the device. The product was sold under unknown conditions, so it's unclear which retailers or dates are affected.
Check for the certification label and safety instructions. If missing, contact IDS LTD for further instructions.
We’ve drafted a message you can send IDS LTD to request your refund or repair — edit it as you like.
Subject: Recall Z-0804-2025 — IDS LTD IDS LTD Hello, I own a IDS LTD that is covered by recall Z-0804-2025 from IDS LTD. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
