---
title: "Daavlin Distributing Company Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Daavlin Distributing Company recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/daavlin-distributing-company/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Daavlin Distributing Company recall records

**6** reported ongoing

6 records in this archive. Latest source date Mar 5, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Mar 5, 2026 FDA device enforcement

### [Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders](https://isitonrecall.com/recall/fda-device-z-2742-2026-photera-400-phototherapy-device-ultraviolet-lamp-for-dermatologic-disorders/)

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).

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2742-2026%22)

Mar 5, 2026 FDA device enforcement

### [Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders](https://isitonrecall.com/recall/fda-device-z-2743-2026-photera-600-phototherapy-device-ultraviolet-lamp-for-dermatologic-disorders/)

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).

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2743-2026%22)

Mar 5, 2026 FDA device enforcement

### [Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders](https://isitonrecall.com/recall/fda-device-z-2744-2026-photera-600-3-d-phototherapy-device-ultraviolet-lamp-for-dermatologic-disorders/)

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).

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2744-2026%22)

Dec 10, 2025 FDA device enforcement

### [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...](https://isitonrecall.com/recall/fda-device-z-2295-2026-phothera-200-phototherapy-devices-indicated-for-use-to-treat-diagnosed-skin-disorders-such-as-but-no/)

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

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, b...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2295-2026%22)

Apr 26, 2022 FDA device enforcement

### [1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. Models: (1 Ser CX 305-4 120-240V 50/60Hz, item # 06OS0004CX6)...](https://isitonrecall.com/recall/fda-device-z-1073-2022-1-series-cx-phototherapy-units-equipped-with-daavlin-s-clearlink-control-system-software-versions-v3/)

Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, ...

[Official source for 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1073-2022%22)

Apr 26, 2022 FDA device enforcement

### [4 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. M4 Ser CX 311-20 120-240V 50/60Hz, item # 807QS0020CX6.](https://isitonrecall.com/recall/fda-device-z-1074-2022-4-series-cx-phototherapy-units-equipped-with-daavlin-s-clearlink-control-system-software-versions-v3/)

Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, ...

[Official source for 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1074-2022%22)

## Reasons in these listed records

- 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).
- Some of the Calibration/Output Certificates had the outputs reversed.
- Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.

These examples come from this result page and are not a ranking of every recall reason.

## Checking Daavlin Distributing Company

### Is there a recall on daavlin distributing company right now?

This archive contains 6 records, including 6 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search Daavlin Distributing Company](https://isitonrecall.com/check/?q=Daavlin%20Distributing%20Company) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
