FMCG
2 min
by Dagmar Moreside

Approved, printed… recalled: The consumer packaging risk no one catches

consumer packaging recall risk

The defect was there from version one. It survived artwork review, stakeholder sign-off, and print approval. This webinar shows exactly how that happens and what it takes to catch errors before they reach the shelf.

~40%
of FDA food and skincare recalls are caused by undeclared allergens — the single biggest trigger
US FDA recall data, discussed in webinar
82
allergens must now be disclosed under new EU regulation — driving a wave of repackaging
EU allergen legislation, discussed in webinar
100%
of the packaging failures discussed in this webinar passed every standard approval step first
That’s the point.
The gap no one talks about

Your process works. Until it doesn’t.

Packaging teams in FMCG work hard to get things right. Artwork goes through rounds of review. Stakeholders sign off. Checklists get ticked.

But most approval processes rely on human eyes checking against earlier versions — and human eyes miss things. A font weight shifts. A regulatory claim drops a word. A barcode degrades. None of it looks wrong until something goes wrong.

Version two gets approved. The team moves to version four. And the deviation travels with the file all the way to print.

This webinar digs into where those gaps live, why standard review processes can’t close them, and what “actually caught” looks like in practice.

What's covered:
1. The reality of packaging risk

What regulators, insurers, and consultants actually see — from undeclared allergens to mislabeled cosmetics — and why the complexity keeps growing.

2. When workflows fail

How multi-version reviews, cross-functional sign-offs, and time pressure create the conditions for error — even when everyone is following the process.

3. The business impact of catching it late

Reprints. Recalls. Retailer penalties. Regulatory challenges. What it actually costs when an error reaches the shelf — and what ROI looks like when you close the gap early.

"The more checks you have, the decrease in accuracy. Especially when you're dealing with very cross-functional teams spread across geographies and departments."

Dagmar Moreside

Strategic Business Development Manager, Schlafender Hase

Meet the speakers:

Dagmar Moreside

Strategic Business Development, CPG/FMCG Lead, Schlafender Hase

Leads GTM strategy at Schlafender Hase, translating CPG/FMCG packaging artwork pain points into content verification use cases. Host & moderator.

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Olivia Santoni

Director, Bloom Regulatory

Olivia advises Beauty & Personal Care, Food & Beverage, and OTC brands on regulatory compliance across multiple markets. Her work includes INCI compliance, EU and UK regulatory frameworks, claims substantiation, and label review for complex and allergen-sensitive products.

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