Corrective Action

Corrective Action
2009 Michigan State University licensed under CC-BY-SA, original at http://www.fskntraining.org.
Basic Level Requirements for

Food Manufacture
y
The organisation shall ensure that

corrective action be undertaken as soon
as possible to prevent further occurrence
of non-conformity.
Presentation Outline
Definitions
y Corrections
y Corrective Actions
y Management and Records
y
Definitions
y
Correction
Action to eliminate a detected nonconformity.
Corrective Action
Action to eliminate the cause of a detected
nonconformity or other undesirable situation.
Corrections
y
A correction relates to the handling of potentially

unsafe products, and can therefore be made in
conjunction with a corrective action.
A correction may be:

Reprocessing
Further processing
Elimination of the adverse consequences of the
nonconformity (such as disposal for other use or
specific labeling)
Corrections need to be pre-planned if possible.

Corrective Actions
y
There can be more than one cause for a

nonconformity that must be addressed in
a corrective action.
Corrective Action:
Includes cause analysis
Is taken to prevent recurrence
Should be preplanned to the extent possible
Corrective Action Components

To correct and eliminate the cause of the
non-conformity (deviation) and restore
process control.
y To identify the product that was
produced during the process deviation
and determine its disposition.
y
How to Detect Nonconformity?

Must have well-planned monitoring
procedures for important parameters
that control food safety hazards.
y Monitoring procedure should specify:
y
Type of monitoring procedures (what)

Procedures used for monitoring (how)
Frequency or maximum time lapse between
application of monitoring procedures (when)
Identify person(s) responsible for conducting
the monitoring procedures (who)
Monitoring and Sampling

y
Continuous inspection
Automated equipment, sensors, supervision
Monitor (for example)
x
x
x
x
Temperature
Time
pH
Moisture
Provides assurance that all products produced

have met criteria for acceptability
Monitoring and Sampling

y
Discontinuous inspection/attribute
sampling
Used to:
x Test ingredients (raw materials)
x Troubleshoot out-of-control process
x Spot check continuous system
Statistical sampling of product lot for a defect

Probability of detection related to defect level
of sampled lot
Limited assurance
Example of Process Monitoring
Requirements in ISO 22000:2005

Planned corrections and corrective
actions to be taken when nonconformities occur shall be specified in
the food safety program to the extent
possible.
y The actions shall ensure that:
y
the cause of the nonconformity is identified,

the parameter(s) is (are) brought back under
control, and
Recurrence is prevented.
ISO 22000:2005
Corrections and control of nonconforming
product:
y A documented procedure shall be
established and maintained defining:
The identification and assessment of affected
end products to determine their proper
handling
A review of the corrections carried out
Corrections
y
All corrections shall be:

Approved by the responsible person(s)
Recorded together with information on the
nature of the nonconformity, its cause(s) and
consequence(s), including information needed
for traceability purposes related to the
nonconforming lots.
Management of Corrective
Actions
Data derived from the monitoring of
critical processes must be evaluated by
designated person(s) with sufficient
knowledge and authority to initiate
corrective actions.
y Corrective actions shall be initiated when
there is a lack of conformity with
established parameters for product safety
or suitability.
y
Management of Corrective
Actions
y
The organization shall establish and

maintain documented procedures that
specify appropriate actions to identify and
eliminate the cause of detected
nonconformities, to prevent recurrence,
and to bring the process or system back
into control after nonconformity is
encountered.
ISO 22000:2005 Corrective

Actions
y
(Continued) These actions include:
Reviewing nonconformities (including customer

complaints)
Reviewing trends in monitoring results that may
indicate development towards loss of control
Determining the cause(s) of nonconformities
Evaluating the need for action to ensure that
nonconformities do not recur
Determining and implementing the actions
needed
Recording the results of corrective actions taken
Reviewing corrective actions taken to ensure that
they are effective.
Records
y
Records for corrective actions and

nonconformities must include:
The actual production records for the product
A standard form listing the following:
x Hold number, deviation, reason for hold, date and code
of product held, name of responsible individual
Authority recommendations on final disposition

of product in question
Accurate accounting of all units in question
Statement of the procedure for handling the
nonconformity
Questions?
License to Reuse
y
2009 Michigan State University, licensed under

Creative Commons Attribution-Share Alike 3.0
Unported (CC-BY-SA).
Source: 2009 Michigan State University, original at

http://www.fskntraining.org, licensed under Creative
Commons Attribution-Share Alike 3.0 Unported.
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What is the difference between a correction and a corrective action?

What is the difference between a correction and a corrective action?

What are the components of a corrective action?

What are the components of a corrective action?

Corrective Action

2009 Michigan State University licensed under CC-BY-SA, original at http://www.fskntraining.org.

Basic Level Requirements for

The organisation shall ensure that

2009 Michigan State University licensed under CC-BY-SA, original at http://www.fskntraining.org.

2009 Michigan State University licensed under CC-BY-SA, original at http://www.fskntraining.org.

2009 Michigan State University licensed under CC-BY-SA, original at http://www.fskntraining.org.

A correction relates to the handling of potentially

A correction may be:

Corrections need to be pre-planned if possible.

There can be more than one cause for a

2009 Michigan State University licensed under CC-BY-SA, original at http://www.fskntraining.org.