Valeda Light Delivery System for dry age-related macular degeneration was shipped with EU electrical configuration that won't plug into standard U.S. outlets. Affected units have specific serial numbers and lot codes.
U.S. customers were shipped devices that were configured for the European Union and were unable to plug the device in the electrical outlet.
Valeda's Light Delivery System for dry age-related macular degeneration was recalled because some units were configured for European electrical outlets and won't work with standard U.S. outlets. This means the device cannot be used properly in the United States.
The device was shipped with European electrical configuration that doesn't match standard U.S. outlets. This means the device cannot be plugged in or used in the United States, so it won't function for its intended purpose.
U.S. customers who purchased the Valeda Light Delivery System for dry age-related macular degeneration between certain dates. People using the device for macular degeneration treatment are most at risk of not being able to use it properly.
Check for serial numbers 20166-20178 on the device. The product was sold with specific lot codes including UDI-DI +B749200001030/$$+720166/16D20250311W through UDI-DI +B749200001030/$$+720178/16D20250311Z.
Verify if your device has a European electrical configuration that won't plug into standard U.S. outlets by checking the serial number on the device.
The device was shipped with European electrical configuration that doesn't match standard U.S. outlets, so it cannot be used properly in the United States.
Check for serial numbers 20166-20178 on the device. The product was sold with specific lot codes including UDI-DI +B749200001030/$$+720166/16D20250311W through UDI-DI +B749200001030/$$+720178/16D20250311Z.
The device cannot be used in the United States due to the electrical configuration issue, but there is no specific remedy stated in the recall notice.
We’ve drafted a message you can send Valeda to request your refund or repair — edit it as you like.
Subject: Recall Z-2046-2025 — Valeda Valeda Hello, I own a Valeda that is covered by recall Z-2046-2025 from Valeda. 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.
