Daavlin recalls Phothera 200 phototherapy devices with model numbers 210NDT4 and 210NCL4 where calibration certificates had outputs reversed. Affected units include specific serial numbers listed in the recall notice.
Some of the Calibration/Output Certificates had the outputs reversed.
Daavlin is recalling Phothera 200 phototherapy devices that treat skin conditions like psoriasis and eczema. Some units had calibration certificates with reversed output settings, which could lead to incorrect treatment doses if used without correction.
The calibration certificates for some units had the output settings reversed. This could cause incorrect light doses during treatment, potentially leading to ineffective therapy or skin damage if not corrected.
People who own or use Phothera 200 devices with model numbers 210NDT4 or 210NCL4 and the listed serial numbers are affected. Patients using these devices for skin conditions under a physician's supervision are most at risk.
Check if your device has model numbers 210NDT4 or 210NCL4 and one of the listed serial numbers. The recall includes specific serial numbers starting with '2-03' followed by 10 digits.
Identify your device's model number (210NDT4 or 210NCL4) and compare with the listed serial numbers.
Some calibration certificates had reversed output settings, which could lead to incorrect treatment doses.
No, but you should check if your device is affected by comparing the model and serial numbers to the list provided.
Check if your device has model numbers 210NDT4 or 210NCL4 and one of the specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Daavlin to request your refund or repair — edit it as you like.
Subject: Recall Z-2295-2026 — Daavlin Daavlin Hello, I own a Daavlin that is covered by recall Z-2295-2026 from Daavlin. 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.
