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Louisiana Department of Health & Hospitals | Bruce Greenstein, Secretary

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FDU Guidance Document-Food Processing Plans and Recall Plans

New Regulations in Part VI, title 51, L.A.C.

For General Manufacturing Firms Processing Plans:

  • Plans must be written, implemented, and maintained up-to-date with any changes made to the firm's operational procedures.
  • Plans must be available for review by your inspector upon request.
  • Plans must include the following elements:
    • list of steps in process, including potential biological, physical, chemical, or radiological hazards that may be introduced at each step;
    • description of controls used to address the hazards listed above;
    • description of methods used to monitor the controls noted above;
    • records of corrective actions taken as a result of monitoring above;
    • and records of changes to plan as a result of corrective actions documented above.

NOTE: If a HACCP plan is currently in use, a separate food processing plan is not required.

Recall Plans:

  • Plans must be written and available for review by your inspector upon request.
  • Plans must have a provision to notify your inspector and/or the Central Office staff of the Food and Drug Unit in the event of a product recall. If goods are shipped interstate, additional provisions must be made to notify the local or regional federal Food and Drug Administration office.
  • Plans must include the following elements: 
    • identity of products including brand name and lot/batch code;
    • reason for recall;
    • date and means of discovery of the reason;
    • total affected product produced and amount estimated to be in distribution;
    • list of consignees that may have received affected product;
    • contact information for the firm's recall coordinator;
    • and, proposed strategy for conducting the recall, including media notifications, method of evaluating whether the recall needs to occur at the level of wholesale distribution, retail distribution, or the consumer; method of checking the effectiveness of the recall, including follow-up store visits or telephone/email contacts; method of determining whether changes to the plan are warranted by the results of the effectiveness checks.

For Ice-Vending Unit Operators

Processing Plans:

  • Plans must be written and posted in a waterproof container (along with the cleaning and maintenance information) in the unit.
  • Processing plans should consist of an outline of the operating protocol of the unit, including the following items:
    • a process flow showing steps water goes through from the source input to finished bag or discharge; 
    • any identifiable hazards water may encounter along the above path; 
    • any controls or preventative measures in place in the unit to control the above hazards (e.g., cut-off switches, UV, filtration, et cetera); 
    • records of monitoring (including, for example, testing of product water for biological contaminants) efficacy of controls listed above; 
    • records of corrective actions (including replacement of parts relating to controls) resulting from monitoring of items listed above;

Recall Plans:

  • Plans must be written and available for review by your inspector upon request.
  • Plans must have a provision to notify your inspector and/or the Central Office staff of the Food and Drug Unit in the event of a product recall. If goods are shipped interstate, additional provisions must be made to notify the local or regional federal Food and Drug Administration office.
  • Plans must include the following elements: 
    • identity of products including brand name and lot/batch code;
    • reason for recall;
    • date and means of discovery of the reason;
    • total affected product produced and amount estimated to be in distribution;
    • list of consignees that may have received affected product;
    • contact information for the firm's recall coordinator;
    • and, proposed strategy for conducting the recall, including media notifications, method of evaluating whether the recall needs to occur at the level of wholesale distribution, retail distribution, or the consumer; method of checking the effectiveness of the recall, including follow-up store visits or telephone/email contacts; method of determining whether changes to the plan are warranted by the results of the effectiveness checks.