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Daavlin Distributing Company recalls

RecallSweep is tracking 4 recall notices naming Daavlin Distributing Company in the last 180 days, issued by FDA. The most recent is dated July 22, 2026 and the oldest in this window June 10, 2026. They cover Medical Devices.

This page lists what the issuing agencies published. It is not a statement about Daavlin Distributing Company beyond those notices — open each official notice for the authoritative detail.

Recall notices naming Daavlin Distributing Company

4 recalls.

FDA Class II Medical Devices

Daavlin Distributing Company: Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Affected quantity: 212 units

Hazard
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).

Details
Distribution: US Nationwide distribution.. Recall #Z-2744-2026, initiated 20260305. Voluntary: Firm initiated.

Products affected
Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Recall status
Ongoing

FDA Class II Medical Devices

Daavlin Distributing Company: Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Affected quantity: 2 units

Hazard
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).

Details
Distribution: US Nationwide distribution.. Recall #Z-2742-2026, initiated 20260305. Voluntary: Firm initiated.

Products affected
Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Recall status
Ongoing

FDA Class II Medical Devices

Daavlin Distributing Company: Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Affected quantity: 26 units

Hazard
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).

Details
Distribution: US Nationwide distribution.. Recall #Z-2743-2026, initiated 20260305. Voluntary: Firm initiated.

Products affected
Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Recall status
Ongoing

FDA Class II Medical Devices

Daavlin Distributing Company: Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vi…

Affected quantity: 368 units

Hazard
Some of the Calibration/Output Certificates had the outputs reversed.

Details
Distribution: US Nationwide distribution.. Recall #Z-2295-2026, initiated 20251210. Voluntary: Firm initiated.

Products affected
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4

Recall status
Ongoing

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