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Is Modified Food Starch Banned in Europe?

3 min read

Modified food starch is not banned in Europe, but its use is strictly regulated. All modified starches used as food additives in the European Union must undergo rigorous safety testing and receive authorization from the European Food Safety Authority (EFSA) before they can be added to food products.

Quick Summary

An examination of the legal status of modified food starch within the European Union. Analysis of EU regulations, the role of EFSA, E numbers assigned to approved starches, and consumer information on these common food additives.

Key Points

  • Modified starch is not banned in Europe: Specific types of modified food starch are legally permitted for use in the EU.

  • Strictly regulated, not prohibited: The European Union uses a 'positive list' system, meaning only additives that have undergone and passed a rigorous safety evaluation are authorized for use.

  • European Food Safety Authority (EFSA) oversight: EFSA is the scientific body that carries out safety assessments and re-evaluations of all food additives, including modified starches.

  • E numbers for identification: Approved modified starches are identifiable on ingredient lists by their E numbers, such as E1404 or E1422, offering transparency to consumers.

  • Not genetically modified: It's crucial to distinguish between 'modified food starch' and 'genetically modified' ingredients; the modification process does not involve genetic engineering.

  • Rigorous safety testing required: Before any modified starch is approved, it must be scientifically proven to be safe for human consumption and have a demonstrable technological function.

In This Article

European Regulation of Modified Food Starch

Contrary to a common misconception, modified food starch is not banned across Europe. Instead, the European Union maintains a strict and comprehensive framework for the approval and use of all food additives, including modified starches. The primary legislation governing this is Regulation (EC) No 1333/2008 on food additives, which outlines the conditions under which an additive can be authorized.

For a modified starch to be used in EU food products, it must meet specific criteria. First and foremost, it must not pose a health risk to consumers based on available scientific evidence. Second, it must fulfill a demonstrable technological need that cannot be achieved by other means. Lastly, its use must not mislead the consumer. This process ensures that authorized additives are both safe and necessary.

The Role of the European Food Safety Authority (EFSA)

The European Food Safety Authority (EFSA) is the key body responsible for evaluating the safety of all food additives in the EU. For modified starches, this has involved multiple re-evaluations to ensure they remain safe under changing conditions and with new scientific information. A notable re-evaluation in 2017 concluded that a dozen specific modified starches posed no safety concerns at the reported use levels for the general population. EFSA reviews extensive data, including short- and long-term toxicity studies, to make its conclusions. This continuous oversight is a crucial element of the EU's proactive approach to food safety.

E Numbers for Approved Modified Starches

To identify approved food additives, the European system uses a numbering system known as E numbers. Modified food starches are assigned numbers in the E14xx series, making them easily identifiable on ingredient lists. This labeling requirement promotes transparency and allows consumers to make informed choices. Some examples of commonly used E-numbered modified starches include:

  • E1404: Oxidized starch
  • E1412: Distarch phosphate
  • E1414: Acetylated distarch phosphate
  • E1422: Acetylated distarch adipate
  • E1442: Hydroxypropyl distarch phosphate

Each of these specific starches has undergone EFSA evaluation and is authorized for use in specified foods at certain levels, demonstrating that authorization is not a blanket approval but a precise regulatory process.

The Distinction: Modified vs. Genetically Modified

It is important to clarify a frequent point of confusion: 'modified food starch' is not the same as a 'genetically modified organism' (GMO). While the raw materials for some modified starches may come from crops like maize, the modification process itself is a physical, enzymatic, or chemical alteration of the starch, not a genetic engineering process. Furthermore, EU regulations on GMOs are separate and distinct, requiring strict authorization and labeling. In Europe, the agricultural raw materials used in starch production are conventional and non-GMO.

Comparison: Regulation of Modified Starch (EU vs. USA)

To better understand the European approach, it's useful to compare it with the system in the United States.

Feature European Union (EU) United States (USA)
Regulatory Body European Food Safety Authority (EFSA) Food and Drug Administration (FDA)
System of Approval Positive List System: Only additives explicitly approved and listed in EU regulations (e.g., Regulation (EC) No 1333/2008) are permitted. Generally Recognized as Safe (GRAS): Additives are either explicitly approved or deemed safe through scientific consensus, a less formal process for some substances.
Labeling All food additives must be listed by function and E number or specific name (e.g., "Modified Food Starch E1422"). Additives are listed by common name or "food starch-modified".
Focus Prioritizes precautionary principle, requiring proof of safety before use. Emphasis on historical use and scientific consensus for GRAS status.

Conclusion

In conclusion, the claim that modified food starch is banned in Europe is incorrect. The European Union permits the use of specific modified food starches, but only after they have been rigorously assessed for safety by the European Food Safety Authority (EFSA) and included on a positive list of authorized food additives. These approved starches are identified by their E numbers on ingredient lists, providing consumers with clarity. This highly regulated approach, distinct from the system in the United States, emphasizes consumer protection and technological necessity for all authorized food additives. The regulation of modified food starch serves as a prime example of the EU's strict food safety standards.

More Resources on EU Food Additives

For a complete list of authorized additives and detailed regulatory information, refer to the official EU legislation on food additives.

Regulation (EC) No 1333/2008 of the European Parliament and of the Council

Frequently Asked Questions

No specific type of modified food starch is outright banned, but any starch that has not passed the strict safety assessment by the European Food Safety Authority (EFSA) and been included in the official positive list cannot be used in EU food products.

No, the two are not the same. 'Modified' in this context refers to a physical, enzymatic, or chemical process that alters the starch's properties. Separate, much stricter regulations apply to genetically modified ingredients.

Under EU labeling laws, all approved food additives, including modified starches, must be listed on the ingredient label. They are identified by their function (e.g., thickener) followed by their specific E number (e.g., E1422).

The modification process improves the starch's functional properties for use in processed foods. This can include enhancing its ability to withstand heat and acid, improving its texture, and increasing its stability for freezing and thawing.

The European Food Safety Authority (EFSA) is the body responsible for scientifically evaluating and ensuring the safety of all food additives, including modified starches, before they can be authorized for use in the European Union.

In Europe, products derived from GMOs are subject to separate authorization and labeling requirements. While a modified starch could theoretically originate from a GMO crop, the EU has strict regulations and testing in place to ensure compliance.

No, the regulatory systems are different. The EU uses a positive list system requiring pre-market approval, while the US uses a system that includes both pre-market approval and the Generally Recognized As Safe (GRAS) designation.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.