Tag Archives: product sampling

Rodrigo Malig
Ask The Expert

Why Customized Food Safety Programs Featuring AI and Molecular Testing Are Essential

By Food Safety Tech Staff
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Rodrigo Malig

Everyone understands the importance of a robust food safety program. It should ensure the safety of the product and environment, backed by solid, traceable data. The food industry is vast, stretching from the farm all the way to our plates, and includes a diverse array of foods and drinks. Different segments of this industry have specific needs, whether it’s unique spoilage tests or specialized predictions based on distinct data. Unfortunately, current services haven’t delivered a trustworthy solution for these needs.

Rodrigo Malig is the Chief Product Officer at TAAG Genetics. He oversees both the artificial intelligence and molecular diagnostic teams. In this column, Rodrigo discusses the crucial roles of AI and molecular testing in crafting a reliable, tailored solution for food safety.

What are common deficiencies in current food safety and quality programs?

Malig: Common shortcomings in Food Safety and Quality programs (and frustrations for hardworking FSQA professionals) include:

Lack of Customization: Many programs don’t adapt or customize to specific industry needs.

Routine Sampling Issues: Environmental sampling is often random, lacking intelligent risk-based criteria. There’s also an insufficient adaptive process after each sampling cycle.

Paper files
Relying on paper files makes keeping track of data, trending it and analyzing it more difficult and time consuming.

Testing Targets: The targets for environmental and finished product testing are often insufficient. For instance, industries need specific tests for spoilage microorganisms, but many don’t have access to these tests and rely instead on general aerobic plate counts, and yeast and mold.

LIMS (Laboratory Information Management System) Limitations: These systems often don’t offer accurate digitized mapping, customization or ability to adapt, leading them to inaccurately represent a facility or its changing needs.

Outdated Methods: Some programs still rely on outdated technologies and methods. Let’s take plate counts for example. There’s a focus on mere quantitative results without the specificity of what those organisms are. This prevents facilities from taking precise corrective and preventive actions. Additionally, we all know plate counts can be time consuming with long incubation times, have limited sensitivity, lack genetic information, require manual labor (thereby creating additional risk for contamination) and increase overall costs. It is essential to determine when plate counts need additional support or substitution, such as with PCR (Polymerase Chain Reaction).

Comparison to FDA Standards: Many confirmation methods are inferior compared to the FDA’s Whole Genome Sequencing.

PCR Kit Issues: When using PCR, many kits test for only a single microorganism. This limitation requires multiple tests to be run, leading to increased turnaround times and costs.

Traceability Concerns: A significant deficiency is the lack of traceability in many programs, requiring additional documentation to be performed on paper.

Incomplete data and analysis: Antiquated data management systems result in insufficient data collection and digitization. Many in the industry still manually write on paper or use Excel spreadsheets, which makes keeping track of data, trending it and analyzing it more difficult and time consuming.

Reactive and not predictive: Because of the deficiencies detailed above, food safety programs become reactive and insufficient to address risk.

How can we improve current food safety and quality programs?

Malig: An improved food safety and quality program must become predictive (and not reactive), by embracing and implementing technology featuring customization, molecular testing and AI. Below is a basic checklist for food companies to follow:

Data analysis smartphone
An ideal food safety and quality program should be digital, implement artificial intelligence and molecular testing, be comprehensive, and most importantly be simple and mobile!

Customized Software & Testing: Utilize software and tests tailored to your unique requirements.

Advanced Environmental Sampling: Embrace sampling that’s customized, risk-based, predictive and adaptive. Employ digitization and AI to efficiently map, record, analyze and predict sampling schemes. This system should also adapt after each cycle and accommodate changes in the environment, equipment and processes.

Molecular Testing: Polymerase Chain Reaction (PCR) testing is a molecular biology technique with several advantages, including:

  • Sensitivity: PCR is highly sensitive and can detect very small amounts of genetic material (DNA or RNA) in a sample. This makes it effective for detection even when the pathogen is present in low concentrations.
  • Specificity: PCR is highly specific, meaning it can accurately identify and differentiate between different microorganisms or genetic variants. This specificity reduces the likelihood of false-positive results.
  • Speed: PCR can provide results relatively quickly, often within a few hours, depending on the type of PCR used (e.g., real-time PCR or RT-PCR). This rapid turnaround time is crucial for time sensitive decisions in the food industry.
  • Cost: PCR can be cost efficient, especially with multiplex PCR kits that detect multiple pathogens in a single reaction, which essentially cuts time, labor, use of lab equipment and space, and overall cost.

Industry-Specific Microorganism Testing: Ensure you’re testing for microorganisms relevant to your industry, processes and products. This is especially crucial if your products are susceptible to spoilage by specific microorganisms.

Adaptive LIMS: Your Laboratory Information Management System (LIMS) should be both customizable and adaptive. It should digitally represent your facility with accuracy and adapt to any changes or needs.

Dynamic Microbiological Programs: Move away from reactive and repetitive testing schemes. Most current microbiological programs tend to test the same samples repeatedly. With the help of AI algorithms, we can now implement preventive and risk-based microbiological programs.

This real-life case study illustrates how a Fortune 100 Company implemented the solutions above to improve their food safety and quality program.

TAAG Contact Us

 

Baby Bottle

Stratified Sampling Increases Cronobacter Identification in Infant Formula

By Food Safety Tech Staff
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Baby Bottle

A new study, published in the Journal of Food Protection, found that spacing out samples over time, called “stratified” sampling, is better at catching risky pathogens like Cronobacter in powdered products, such as infant formula, than randomly sampling from the product as it is being produced. In addition, the study found that that while taking more samples of a product generally increases the chance of catching the pathogen, there is a point after which it is unlikely that additional sampling will increase safety.

The new paper “Simulation Evaluation of Power of Sampling Plans to Detect Cronobacter in Powdered Infant Formula Production” used computer models to simulate sampling and testing finished formula, to determine the efficacy of current national and international guidelines for testing programs, and find solutions to improve detection of Cronobacter in these types of products.

All efforts were based on detecting a realistic hazard, here defined by testing samples from Cronobacter-contaminated batches produced in Europe in the 2010s, using the most current data available. The paper found that safety plans with 30 or more grab samples had a very high probability of detecting the hazard. And that there was a point of diminishing returns, such that very high sample numbers—for example, testing every can produced—would not be meaningfully more powerful.

“This shows that existing sampling and testing guidance is powerful, at least for the one hazard profile our team had access to for the study,” said project lead Matthew J. Stasiewicz of the University of Illinois Urbana-Champaign. “This also highlights the need for additional research and data-sharing efforts into patterns of contamination in current infant formula production, so that sampling and testing can be better matched to current needs.”

“In additional to analyzing scenarios we found relevant, we built a web app that allows industry stakeholders to simulate various sampling scenarios and gain deeper understanding of the effectiveness of sampling plans specific to their plants. With this knowledge, producers can proactively address risks and optimize current sampling practices,” added Minho Kim, lead author.

 

Recall

JBS Recalls Nearly 5000 Pounds of Imported Australian Boneless Beef Due to Potential E. Coli Contamination

By Food Safety Tech Staff
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Recall
JBS Boneless Beef product
Label of recalled JBS Australia beef product. (Image from FSIS)

JBS USA Food Company is recalling about 4,860 pounds of imported raw and frozen boneless beef products over concern of contamination with E. coli O157:H7. The products were imported on or around November 10, 2020 and shipped to distributors and processors in New York and Pennsylvania.

The issue was uncovered during routine product sampling collected by FSIS, which confirmed positive for the presence of E. coli O157:H7, according to an FSIS announcement. “FSIS is concerned that some product may be frozen and in cold storage at distributor or further processor locations,” the announcement stated. “Distributors and further processors who received these products are urged not to utilize them.”

No illnesses or adverse reactions have been reported.