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Quanta System, S.p.A Recalls
6 recalls on record · January 23, 2013 to June 16, 2021 · Medical Devices
Recalls by year
13
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 16, 2021Medical DevicesFDA
Quanta System, S.p.A. recalls Quanta System Sterile Optical Laser Fiber, reusable
Hazard: Product sterility is potentially compromised.
June 16, 2021Medical DevicesFDA
Quanta System, S.p.A. recalls Quanta System Sterile Optical Laser Fiber, single use
Hazard: Product sterility is potentially compromised.
June 16, 2021Medical DevicesFDA
Quanta System, S.p.A. recalls Olympus Sterile Optical Laser Fiber, single use and reusable
Hazard: Product sterility is potentially compromised.
January 23, 2013Medical DevicesFDA
Quanta System, S.p.A. recalls Ultrawave II EX 1320/ Ultrawave III EX 1320 Powered Laser Surgical Instrument. Nd:YAG 1064 nm: Coagulation and hemostas
Hazard: Quanta System S.p.A, Italy, is notifying U.S. consignees that their website contained promotional materials for products distributed in the U.S. which did not specify that some of the claims made therein were not meant to apply to the U.S. distributed devices.
January 23, 2013Medical DevicesFDA
Quanta System, S.p.A. recalls Eterna Giovinezza System, Powered Laser Surgical Instrument. Permanent hair reduction; Photocoagulation of dermatolog
Hazard: Quanta System S.p.A, Italy, is notifying U.S. consignees that their website contained promotional materials for products distributed in the U.S. which did not specify that some of the claims made therein were not meant to apply to the U.S. distributed devices.
January 23, 2013Medical DevicesFDA
Quanta System, S.p.A. recalls Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and pigmented les
Hazard: Quanta System S.p.A, Italy, is notifying U.S. consignees that their website contained promotional materials for products distributed in the U.S. which did not specify that some of the claims made therein were not meant to apply to the U.S. distributed devices.