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
- 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