FDA recall record

Theralase TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee recall — FDA Z-0606-2020

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

Class IIIclassification
Z-0606-2020official record ID
Dec 11, 2019report date

Recall record at a glance

Official recordZ-0606-2020
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTheralase Inc.
Report dateDec 11, 2019
Recall initiation dateSep 26, 2019
Quantity41 units
LocationEast York, Canada

Official product description

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

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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