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U.S. Department of Health and Human Services

Class 2 Device Recall Sunnex

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 Class 2 Device Recall Sunnexsee related information
Date Initiated by FirmFebruary 13, 2007
Date PostedJuly 24, 2007
Recall Status1 Terminated 3 on January 06, 2009
Recall NumberZ-1100-2007
Recall Event ID 38075
Product Classification Medical Examination Light - Product Code FTA
ProductSunnex Celestial Star MR-16 (lamp holder) Medical Examination Lighting used in Model Numbers: CS2050C (ceiling mount), CS2050W (wall mount). CS2050D (dual mount) , CS2050M (mobile).
Code Information Units manufactured between May 15, 2006 through October 1, 2006
Recalling Firm/
Manufacturer
Sunnex Inc.
3 Huron Dr
Natick MA 01760-1314
For Additional Information ContactBrian Jacobson
508-651-0009 Ext. 231
Manufacturer Reason
for Recall
Surgical and/or exam lamp holder may malfunction, discolor, melt and smolder.
FDA Determined
Cause 2
Other
ActionSunnex notifiied distributors by letter March 9, 2007. Sunnex is providing replacement product to end users
Quantity in Commerce346 lamps
DistributionNationwide
Total Product Life CycleTPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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