ClearanceBrief
Recall Z-1074-2022 ยท FTC Light, Ultraviolet, Dermatological

Daavlin Distributing Company

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.

DateApr 26, 2022
StatusOpen, Classified
ReasonSoftware issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.
Root causeSoftware Design Change
ActionBeginning April 26, 2022 Daavlin Distributing Co. is sent a recall notification letter via certified mail to customers. Customers are to acknowledge receipt of the notification and a company representative will call customers to arrange for return of the devices to update software. If you have any questions or concerns, contact the company at (800) 322-8546. Monday through Friday, 8:00 AM to 4:30 PM, EST.
Quantity1
DistributionWorldwide 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, NY, OH, OK, OR, PA, SD, TN, TX, VA, WA, WI, WV and the countries of Australia, Canada.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K1111724 SERIES PHOTOTHERAPY UNIT MODEL 4 SERIES
Daavlin Distributing Co., Aug 29, 2011