Inc Class II Coherent

Company: Coherent, Incc
Date of Enforcement Report: 12/22/04
Class: II

PRODUCT
Coherent brand DUO Diode Laser Systems. A Non-medical, class IV industrial materials processing machine. Recall # Z-0360-05.

REASON
Software problem that may cause unintended emission of laser radiation.

CODE
All serial numbers are affected by this recall action. Serial numbers range from 1003 to 1092.

RECALLING FIRM/MANUFACTURER
Coherent, Inc., Santa Clara, CA, by letters on March 30, 2004. Firm initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE
75 units.

DISTRIBUTION
NC, Canada, Germany, and Japan.

About the author

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

SoftwareCPR Training Courses

IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software

ISO 14971 Risk Management (typically with heavy emphasis on software aspect)

IEC 81001-5-1 Cybersecurity Lifecycle

ISO 13485 QMS Requirements & optionally ISO 19011 for leading audits

Being Agile Yet Compliant (AAMI TIR 45)

IEC 29119-1 Software and System Testing

US Classification for Software Devices

IEC 62366 Usability Process and Documentation

Or just email training@softwarecpr.com for more info.

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