Z-0691-2013Class II

Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and...

Name: Z-0691-2013 Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and...
Creator: Quanta System, S.p.A.
Published: 2012-11-07
License: https://open.fda.gov/license/

Quanta System Inc. / initiated 2012-11-07 / Terminated / root cause: labeling and UDI

FDA source

Quanta System, S.p.A. began a recall of Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and pigmented lesions; Hair and tattoo removal; The... on 2012-11-07. FDA classified it as Class II and gives the reason as "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...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-0691-2013
Classification: Class II
Status: Terminated
Initiated: 2012-11-07
Posted: 2013-01-17
Terminated: 2013-01-23
Recalling firm: Quanta System Inc.
Product: Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and pigmented lesions; Hair and tattoo removal; The incision, excision, ablation, vaporization of soft tissue for general dermatology. Ruby 694nm: Cutting, vaporization and ablation of soft tissue; Tattoo removal; Treatment of benign pigmented lesions.
Product code: GEX Powered Laser Surgical Instrument
Reason for recall: 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.
Root cause tag: labeling and UDI
FDA root cause: Labeling False and Misleading
Action: Quanta System sent a letter dated November 7, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to perform the following: quarantine and destroy all promotional literature printed from the manufacturer, website or obtained from the manufacturer. Provide any promotional literature independently produced by the initial importer or distributor containing information about Quanta System products. Provide URL of initial importers or distributors website if information about Quanta System products is contained therein. Provide a written certification that all actions have been taken. Quanta System has or will: review all promotional materials and website information provided by initial importers and distributors; advise initial importers and distributors of any actions that need to be taken to change promotional materials and/or website information. For questions regarding this recall call 303-223-4336.
Quantity in commerce: 75 units
Distribution: Class II Recall - Worldwide Distribution - USA including TX, AZ, OR, and CO. Only US product is affected by this recall.
Product codes and lots: All codes and devices are applicable.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0691-2013
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0691-2013	Class II	Terminated	Voluntary: Firm initiated	2013-01-23	2013-01-17
Z-0692-2013	Class II	Terminated	Voluntary: Firm initiated	2013-01-23	2013-01-17
Z-0693-2013	Class II	Terminated	Voluntary: Firm initiated	2013-01-23	2013-01-17

Product code GEX

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)