FDABridge
← Balik sa blog
Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

FDA Stories #010 — A Thai Coconut Milk Producer Shipped 12 Containers Without Prior Notice

Maneno 'FDA Approved' yalionekana kwenye tovuti ya Kiingereza ya kampuni. FDA haidhibitishi bidhaa za chakula au vituo. Maneno hayo mawili yalikaribia kuwagharimu soko la Marekani.

Koponan ng FDABridgeEne 1, 20262 min na mabasa

A specialty coffee company in Medellín had a beautiful English-language website built for the US market. Great photography, compelling brand story, detailed product descriptions. On the homepage, in a trust badge section, it said: 'FDA Approved.'

The company's web designer had added it to signal credibility. The marketing team approved it. It looked professional alongside their organic certification and fair trade logos.

There was one problem: the FDA does not approve food products. The FDA does not approve food facilities. Using the phrase 'FDA Approved' in connection with a food product is a misrepresentation of the facility's regulatory status.

Nini kilitokea

The FDA monitors websites and online marketplaces for misleading claims. A compliance reviewer flagged the website during a routine review of coffee imports from Colombia. The FDA sent an email to the facility's US Agent — which, at the time, was a mailbox service that took three weeks to forward it.

By the time the company saw the FDA's communication, the response deadline had nearly passed. They contacted us in a panic.

Tulifanya nini

We removed the 'FDA Approved' claim from the website within hours. We drafted a response to the FDA explaining that the claim was a marketing error, not an intentional misrepresentation, and that it had been corrected. We also audited the entire website and their Amazon listing for any other claims that could trigger FDA scrutiny — and found two more: 'clinically tested' (on a food product, which implies a drug claim) and 'prevents heart disease' (a health claim that food products cannot make without FDA authorization).

All three claims were removed. The response was submitted to the FDA within the deadline. No Warning Letter was issued.

Somo

The words you put on your website, your Amazon listing, and your social media are marketing materials that the FDA monitors. 'FDA Approved,' 'FDA Certified,' 'FDA Registered' (as a trust badge implying approval), and any disease prevention or treatment claims on food products are violations. FDA registration is a compliance filing — not an endorsement. If your marketing materials use any of these phrases, take them down now. If you need help auditing your claims, contact fdabridge.com/contact.

Kailangan mo ng tulong sa susunod?

Kailangan ng tulong sa pagpili ng serbisyo?

Ihambing ang mga serbisyo at piliin ang tamang filing path para sa iyong produkto.

Mas marami pang mabasa

Mga kaugnay na artikulo

Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

Alama za Uwekaji Lebo wa Kifaa cha Matibabu: Watengenezaji wa Kigeni Lazima Wajue Nini kwa Kuingia Soko la Marekani

Abr 28, 2026

Uwekaji lebo wa kifaa cha matibabu nchini Marekani unahitaji alama maalum kwa mawasiliano sahihi. Watengenezaji wa kigeni lazima waelewe viwango vya alama vinavyokubalika na FDA kabla ya kusafirisha vifaa kwenda soko la Marekani.

Magbasa pa →
Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

Usajili wa vifaa vya matibabu kwa watengenezaji wa kigeni: Mwongozo wa Mfumo wa Udhibiti wa Marekani

Mar 26, 2026

Watengenezaji wa vifaa vya matibabu wa kigeni lazima waandikishe taasisi zao, orodha ya vifaa vyao, na kulingana na darasa la vifaa kupata idhini ya FDA au idhini kabla ya kusambaza nchini Marekani.

Magbasa pa →
Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

Maswali Kumi ya Kujiuliza Kabla ya Kuajiri Mshauri wa FDA

May 24, 2026

Kuchagua mtoa huduma wa kufuata sheria za FDA ni uamuzi muhimu. Maswali hayo kumi huwasaidia wazalishaji wa kigeni kuwatenganisha washauri wenye uwezo na wale watakaotokeza matatizo ambayo hawawezi kuyatatua.

Magbasa pa →