Daavlin recalls 32 Photera 600 3-D phototherapy devices with serial numbers starting with 6-09... due to incorrect UV sensor calibration that may lead to insufficient UV exposure for skin conditions.
Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000).
Daavlin is recalling 32 Photera 600 3-D phototherapy devices because their UV sensors were miscalibrated. This could mean the devices don't deliver enough UV light for treating skin conditions, potentially leading to ineffective treatment.
The UV sensor in these devices was set to a lower gain value (4/5 instead of 7), causing the device to output fewer UV counts than intended. This means the light therapy may not be strong enough to treat skin conditions effectively.
People using the Photera 609... serial number devices for skin treatments. Those with specific skin conditions requiring UV therapy are most at risk of ineffective treatment.
Check if your Photera 600 3-D device has a serial number starting with 6-09 followed by 10 digits (e.g., 6-09278NB8CL). The full list of affected serial numbers is provided in the recall notice.
Look for the serial number on your device, which starts with 6-09 followed by 10 digits.
The UV sensor was miscalibrated, causing the device to output fewer UV counts than intended (4/5 instead of 7), which may lead to ineffective treatment for skin conditions.
Check if your device has a serial number starting with 6-09 followed by 10 digits, such as 6-09278NB8CL.
The recall notice does not specify a remedy, so you should contact Daavlin for further instructions.
We’ve drafted a message you can send Daavlin to request your refund or repair — edit it as you like.
Subject: Recall Z-2744-2026 — Daavlin Daavlin Hello, I own a Daavlin that is covered by recall Z-2744-2026 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.
