Requester
Name:	SCAR reference #:

Monitoring of dates	Non conform Parts received	Containment Actions implemented	Analysis started	Root Cause identified	Corrective Actions defined	Corrective Actions implemented	Preventive Actions implemented
Date
D1. Team:
Define 8D Team Champion and Team members here.
D2. Failure description:
Reference number? Who is affected? What kind of problem does it is? Why is it a problem? Which products are affected? Where was it detected? When was it detected? How does the defect / non-conformity looks like? Who was involved?
D3. Containment Action(s):	Responsibility (name)	Target date	Implement. date
Add containment actions here e.g. 100% goods outgoing check, sorting at customer, repair, rework, etc. If there is more than one containment action add more lines. Only one containment action per line! Add information of first batch, serial number, etc. shipped with containment effective.
D4. Root Cause(s):	Responsibility (name)	Date of identification
Add root cause(s) here. If more than one root cause add more lines. Only one root cause per line! Add 5 WHY and/or Fishbone diagram for each root cause.
D5. Possible Corrective Action(s)	Responsibility (name)	Target date	Verification date
Define possible corrective actions (one per line) and add information about verification, validation and possible side effects. If possible corrective action won´t become D6 short describe why.
D6. Implemented Corrective Action(s)	Responsibility (name)	Target date	Implement. date
Define implemented corrective actions (one per line) and add information about objective evidence, that corrective action is effectively solving the root cause as well as of implementation (reference papers like work instructions, FMEA extract, quality control plan, etc.). First batch, serial number produced with corrective action.
D7. Preventive Action(s)	Responsibility (name)	Target date	Implement. date
Define implemented preventive actions (one per line) and add information about objective evidence, that preventive action is effectively preventing root cause as well as of implementation (reference papers like work instructions, FMEA extract, quality control plan, etc.). First batch, serial number produced with preventive action implemented.
D8. Final meeting and congratulation to the team	Responsibility (name)	Date of closing
Clearly state if the SCAR / complaint is accepted or declined! Add lessons learned information.