Facility

THE DAAVLIN DISTRIBUTING CO.

3 recall(s) on record — most severe on record: Class II.

Key facts

3recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1526255
Establishment type	Manufacture Medical Device
Location	205 W. BEMENT STREET Bryan, OH, US 43506
Registration status	Active · expires 2026
Parent company	THE DAAVLIN DISTRIBUTING CO. (owner-operator 1526255)
Brand names	4 SERIES

Activity by year

Recalls (3)

Devices registered here (1)

Light, Ultraviolet, Dermatological
Product code FTC (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4630

Recalls & enforcement

Class IIOngoing2026-03-05
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 IIOngoing2025-12-10
Some of the Calibration/Output Certificates had the outputs reversed.
Class IIOngoing2022-04-26
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.

All facilities operated by THE DAAVLIN DISTRIBUTING CO.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “THE DAAVLIN DISTRIBUTING CO. (FEI 1526255) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1526255-the-daavlin-distributing-co/

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