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U.S. Department of Health and Human Services

Class 2 Device Recall PICTOR 3D

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  Class 2 Device Recall PICTOR 3D see related information
Date Initiated by Firm March 21, 2014
Date Posted June 24, 2014
Recall Status1 Terminated 3 on September 26, 2016
Recall Number Z-1866-2014
Recall Event ID 68259
Product Classification PICTOR 3D - Product Code ooo
Product LAP LASER PICTOR 3D Multi Color Laser System
PICTOR 3D is a LAP laser system which uses multi projection format that defines isocenters, field and MLC contours along with a 3D patient view.
Code Information Product Code: 0007569-0001 
Recalling Firm/
Manufacturer		 LAP of America Laser Applications, LLC
161 Commerce Rd Ste 3
Boynton Beach FL 33426-9385
For Additional Information Contact Tom Gaudet
561-416-9250
Manufacturer Reason
for Recall		 While projecting yellow lines it was notice that the yellow projection has the potential to splits into two separate red and green projections. In this case the difference between the red and green projection was up to 2.5mm.
FDA Determined
Cause 2		 Software design
Action LAP of America Laser sent an Urgent safety Information FFST 2014-2-3 via UPS Next Day Air to the customer.
Quantity in Commerce 1 system
Distribution North Carolina
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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