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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

New Star Lasers, Inc.: FDA inspection found that customers who had received devices with promotional material with outside use indications were not notified when labeling was revised to remove these indications.

Agency Publication Date: September 30, 2016
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Affected Products

Product: CT3Plus (a.k.a. CT3PZ); Catalog number: 7300-0038/ 7300-0038-1. Dermatology: For use in dermatology for incision, excision, ablation, and vaporization with hemostasis of soft tissue; For treatment of fine lines and wrinkles; For mild to moderate inflammatory acne vulgaris; For back acne and atrophic scarring, and; For podiatry, (incision, excision, and coagulation of soft tissue), including. matrixectomy, periungal and subungal warts, plantar warts, radical nail excision, and neuroma

Serial numbers CT3Plus: 4009 4023 ABB0271 4030 4016 ABB0900 ABC0363 BBC1457 ABB0862 ABD0757 ABD1363 ABE0101 ABE1258 BBE1875 ABC1193 BBG1209 ABH1818 ABC1067 ABK2803 ABM0371 ABM1206 ABP1160 ABS1067 ACA1652 ACA1790 ACA2139 ACC1485 ACD0843 ACC1158 ACA1333 ABB0388 SEM02 SEM07 ABB0423 ABE1663 4014 UHG01 UHM02 ABS1761 ABC0921 ABF0613 3045 ABM1410 ABC1252. Serial numbers CT3PZ: ACA1011 ABD0501 UKH01-Z ADMS01 ADMS02 ADMS03 ADPA01 ADPA02 ABS1353-Z ADPD02 ADPD03 ADPD04 ADPD05 ADPD06 ADPE01 ADPE02 ABM1999 ADPE06 ADPE05 ADPG01 ABP1509 ADPH01 ADPH02 ADPH04 ADPH05 ADPH06 ADPH07 ADPE04 ADPK01 ADPK04 ADPK05 ADPK07 ADPM03 ADPP02 ADSB01 3023 4004 ACD1006 4002-Z ACD1621-Z ADSP01 UHK01-Z ADSS04 ADTE01 ADTG01 ABS1171-Z ADUE01.

Product: VariaBreeze; Catalog number: 7300-0035-2. Podiatry: ablation, vaporization, incision, excision, and coagulation of soft tissue including matrixectomy, periungal and subungal warts, plantar warts, radical nail excision, and neuromas. The temporary increase of clear nail in patients with onychomycosis (e.g., dermatophytes Trichophyton rubrum and T. mentagrophytes, and/or yeasts Candida albicans, etc.)

Serial numbers: XSB02-VB AESB01 AHSF02 AHSF04 AHSF05 AHSF06 AHSF07 AHSF08 AHTE01 AHSF03 AHTF01 AHTF02 AHTH01 AHTM02 AHTM01 AHTS01 AHTS03.

Product: ReNew (a.k.a. Trio) Dermatology: for use in dermatology for incision, excision, ablation and vaporization with hemostasis of soft tissue; for use in the treatment of fine lines and wrinkles; for treatment of back acne and atrophic acne scars; for treatment of reflux of the great and small saphenous veins associated with varicose veins and varicosities, and; for laser assisted lipolysis

Serial numbers: ABKK03 ABKK04 ABKM02 ABSG01 ABUP01.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 75048
Status: Resolved
Manufacturer: New Star Lasers, Inc.
Manufactured In: United States
Units Affected: 3 products (44 systems CT3Plus; 47 systems CT3PZ; 17 systems; 5 systems)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.