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FDA vs LFGB: 5 Critical Differences for Food Tinplate Cans

FDA vs LFGB: 5 Critical Differences for Food Tinplate Cans

2025-07-30
    • How to Meet Both US & EU Food Safety Standards for Global Sales

       
      For packaging manufacturers and brands selling tinplate food cans to both the US and EU, navigating FDA and LFBG regulations can feel like a balancing act. Even small differences in coating limits, testing protocols, or labeling rules can delay market entry and add compliance costs. In this guide, we break down the 5 critical differences between FDA (US) and LFBG (EU) standards — and share a practical, step-by-step approach to comply with both, so you can expand your global sales with confidence.
       

      Table of Contents

       
    • Quick Answer: What Are the Core Differences?
    • 5 Critical Differences Between FDA & LFBG
    • How to Comply With Both Standards (Actionable Steps)
    • Quick Recap & Next Steps
    •  

       

      Quick Answer: What Are the Core Differences?

       
      FDA (US) and LFBG (EU) have 5 key differences for tinplate food cans:
       
    • Coating migration limits
    • Testing methods
    • Labeling requirements
    • Tin content rules
    • Approval processes
    •  
      The good news? By aligning with the stricter LFBG requirements, you can create tinplate cans that meet both standards — no need for separate production runs.
       

       

      5 Critical Differences Between FDA & LFBG

       
      Aspect FDA (US) LFBG (EU)
      Coating migration limit Maximum 50ppm (for most coatings) Maximum 10ppm (stricter for food contact)
      Testing method Uses “worst-case” food simulants (e.g., 4% acetic acid) Requires 3+ food simulants (covers more food types, including acidic, fatty, and aqueous foods)
      Labeling No mandatory “food-safe” label (compliance is implied) Mandatory “food contact material” label (specific wording required, e.g., “Suitable for food contact”)
      Tin content No upper limit (as long as migration is low) Maximum 200ppm tin in food (from can coating)
      Approval process Self-certification (manufacturer confirms compliance) Third-party testing and documentation required (before market entry)
       
      Practical Insight: LFBG’s stricter 10ppm migration limit means you’ll need to choose high-performance coatings that meet EU requirements — which will automatically exceed FDA’s 50ppm threshold, simplifying your compliance strategy.
       
       

       

      How to Comply With Both Standards (Actionable Steps)

       
      To streamline compliance for both markets, follow these steps:
       
    • Choose coatings with migration limits ≤10ppm: This meets LFBG’s strictest requirement and easily exceeds FDA’s 50ppm threshold.
    • Test with LFBG’s 3+ food simulants: This covers FDA’s “worst-case” testing requirements, so you won’t need separate tests for the US market.
    • Add LFBG-required labels: The EU’s “food contact material” label is widely accepted in the US, so you can use the same packaging for both regions.
    • Limit tin content to 200ppm: This meets both LFBG’s explicit limit and FDA’s implicit requirement for low migration.
    • Complete third-party testing: This satisfies LFBG’s mandatory pre-market approval and provides documentation to support your FDA self-certification.
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      Quick Recap & Next Steps