SEMICONDUCTOR LASER TREATMENT INSTRUMENT
SEMICONDUCTOR LASER TREATMENT INSTRUMENT was recalled on 2 August 2019 under EU Safety Gate alert A12/1144/19. Damage to sight risk reported by Slovakia. The laser beam is too powerful.
| Alert Number | A12/1144/19 |
| Brand | AEDEN |
| Category | Other - - |
| Risk Type | Damage to sight |
| Notifying Country | Slovakia |
| Country of Origin | People's Republic of China |
| Model Number | GD07-W |
| Published | 2 August 2019 |
Risk Description
The laser beam is too powerful. Direct viewing of the laser beam could cause damage to sight.The product does not comply with the relevant European Standard EN 60825-1.
Measures Taken
Type of economic operator to whom the measure(s) were ordered: RetailerCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: 21/04/2019Type of economic operator to whom the measure(s) were ordered: RetailerCategory of measure(s): Warning consumers of the risksDate of entry into force: 21/04/2019Type of economic operator to whom the measure(s) were ordered: RetailerCategory of measure(s): Recall of the product from end usersDate of entry into force: 21/04/2019
Product Description
Semiconductor laser phototherapy device. The product includes a host machine and а nasal treatment probe with a laser. Packed in a box.
👁️ What Should You Do?
This recall involves a damage to sight hazard related to SEMICONDUCTOR LASER TREATMENT INSTRUMENT.
About this risk
This product can cause eye damage due to excessive light emission (e.g., lasers), projectiles, or chemical splash risk.
Recommended action
Stop using the product immediately. If you have experienced eye discomfort, consult an ophthalmologist. Keep the product away from children.
Who is at risk?
All users, especially children who may look directly at bright light sources.