FDA Enforcement Class III Terminated

TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.

Recall: Z-0606-2020 · Reported December 11, 2019

Enforcement

Recall Number
Z-0606-2020
Event ID
84168
Classification
Class III
Status
Terminated
Product Type
Devices
Firm
Theralase Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
December 11, 2019
Initiation Date
September 26, 2019
Classification Date
February 18, 2020
Termination Date
December 3, 2020
Address
41 Hollinger Rd, East York, N/A, Canada

Description

TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.

Reason

Device was shipped without a Unique Device Identification (UDI) label.

Code Info

Serial Numbers: 3015, 3022, 3037, 3040, 3047, 3052, 3055, 3074, 3076, 3080, 3100, 3101, 3102, 3103, 3123, 3127, 3129, 3131, 3132, 3137, 3139, 3155, 3162, 3166, 3171, 3183, 3187, 3200, 3206, 3227, 3245, 3266, 3268, 3293, 3296, 3297, 3305, 3308, 3318, 3321, 3332

Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, LA, MD, MN, NC, NJ, NM, NY, OR, WI and countries of AU, BH, CA, HK, JO, MX, PK, PH.

Quantity

41 units