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Terminated

The PowerLED / X-TEN / VOLISTA Surgical Light Systems are surgical light systems intended to be used to provide visible illumination of the surgical area or the patient. Ceiling surgical light systems typically include one or more arms that are able to rotate 360 degrees around a central axis.

FDA Recall Z-1990-2015 · Posted 2015-07-07

Recall StatusTerminated
Product CodeFSY
Date Initiated2015-05-29
Date Terminated2017-04-07
Product Quantity646 units

Reason for Recall

Maquet Suspension Arms used with PowerLED/X-TEN/Volista Surgical Light Systems may grind at the junction of the suspension arms which can cause paint chips or particles to fall into the surgical field, when the suspension arms are mounted above the surgical table.

Firm Action

Maquet Medical Systems sent an Urgent Medical Device Field Correction letter dated May 29, 2015, to all affected customers via Fedex. The letter identified the product the problem and the action needed to be taken by the customer. The customer was informed that the correction will include inspection of PowerLED / X-TEN / VOLISTA Surgical Light Systems mounted above the surgical table and replacement of the suspension arms if found to be defective. As a remedial measure, pending replacement of the defective suspensions, Maquet personnel will install a protective plastic strip at each junction where the arms are grinding. The correction will be performed by an authorized Maquet Service Technician. The customer will be contacted by a representative of the Maquet Service team to schedule an on-site inspection and possible service of the PowerLED / X-TEN / VOLISTA Surgical Light Systems. If the customer has any questions or require additional information, they can contact their local Maquet representative, or Maquet Customer Service at 1-888-627-8383 (option 3), Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. EST.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution - Nationwide Distribution and to the countries of : Argentina, Austria, Australia, Belgium, Bulgaria, Bahrain, Bolivia, Brazil, Belarus, Canada, Switzerland, Chile, China, Colombia, Croatia, Hungary, Indonesia, Ireland, Iraq, Jordan, Japan, Czech Republic, Germany, Denmark, Ecuador, Egypt, Spain, Finland, France, Greenland, Greece, Hong Kong, United Arab Emirate, United Kingdom, Kenya, Kuwait, Sri Lanka, Luxembourg, Libya, Mongolia, Martinique, Mexico, Malaysia, Namibia, Nigeria, Netherlands, Norway, Oman, Panama, Peru, Philippines, Pakistan, Poland, Saint Pierre and Miquelon, Portugal, Reunion, Romania, Russia, Saudi Arabia, Sweden, Singapore, Slovenia, Slovakia, Senegal, Thailand, Tunisia, Turkey, Trinidad and Tobago, Taiwan, Uruguay, Venezuela, Serbia, Yemen, Mayotte and South Africa.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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