Skip to main content
. 2023 Jan 27;11:e14648. doi: 10.7717/peerj.14648

Table 3. The control measures for storage and pasteurization stages highlighting corrective actions.

Hazard Type of hazard Control measure or corrective actions
– Raw milk must be stored at temperature not more than 10 °C.
– Milk must be adequately heated (for batch pasteurization: 63 °C for 30 min).
Vegetative bacteria growth. – Keep all lines, vessels and valves clean and sanitized with records of the time and date according to recommended frequency (Food & Drug Administration, 2018).
Biological – The product shall be considered to be disposed if the temperature or time are not met within 2 h (Food & Drug Administration, 2018).
– Pasteurizer design and construction must meet the Grade-A Pasteurized Milk Ordinance (Poltronieri & Rossi, 2017).
– Storage vessels must be cleaned after each use (keep records).
Contamination with vegetative bacteria. – Linked valves and lines must be cleaned at least once daily after using them.
– Connected opening and valves must be tightly closed with proper lids. The product-contact surfaces of all multi-use containers, utensils and equipment used in storage shall be effectively cleaned and shall be sanitized before each use (Food & Drug Administration, 2018).
– Ensure adequate separation between the vessels and lines used for the product and lines used for detergents and chemicals (Food & Drug Administration, 2018).
Remaining cleaning and sanitizing chemicals. – To ensure that needed separation is maintained, inter-washes throughout the day can be done (Food & Drug Administration, 2018).
Chemical – Any surface that comes in contact with the product should be sanitized before using every time during processing (examples of contacts surfaces: equipment and tanks used for different purposes) (Poltronieri & Rossi, 2017)
Contamination with allergens from materials mixed with product. – Pipelines, valves, and any part of the pasteurizer used for any other food, that might contain allergens, must be cleaned properly to avoid unlabeled cross contamination (Food & Drug Administration, 2018).