ASA Compliance GroupAmazon Seller Account ReinstatementMedical claims appeal

Amazon medical claims appeal services.We take full ownership of your case.

Amazon flagged medical claims on your listing or packaging? We review the exact wording and product records, then handle the corrections, supporting evidence and appeal.

Founder-led review. Most first replies within about an hour.

Or Shamosh speaking at the European Seller Conference in Prague, March 2025
Or Shamosh, Founder of ASA Compliance Group
European Seller Conference. Prague, March 2025.
  • 5,500+ cases handled
  • 98% historical reinstatement rate
  • Since 2016

Last verified as of .

Amazon Sellers Appeal by Or Shamosh

Amazon Seller Account Deactivated? You’re in Expert Hands.

Founder-led enforcement expertise backed by executive leadership and specialist teams in Seller Central.

Founder, ASA Compliance Group · International speaker on Amazon enforcement and reinstatement

When your Amazon account or listings are suspended, every moment counts, and genuine expertise matters. Or Shamosh, founder of ASA Compliance Group, has spent over 10 years mastering the complexities of Amazon’s policies, compliance guidelines, and seller reinstatements. His LL.B. background informs how he reads Performance Notifications and frames compliance strategy; complex matters still run through ASA Compliance Group’s in-house legal department and outside counsel when required. He has led work across 5,500+ cases. His work spans seller account suspensions, listing appeals and compliance cases.

Or regularly shares his knowledge at seller conferences and webinars worldwide, including Prague March 2025, Sofia April 2025 and April 2026, Warsaw May 2026, with an upcoming UK appearance in October 2026. See conference appearances, explore seller webinars, read the restricted keywords guide, or see client stories in Testimonials.

AmazonSellersAppeal is operated by ASA Compliance Group, with dedicated appeal, legal, IP, and compliance teams in Seller Central. Michael Gourin and Smadar Popovski, alongside Or, lead intake and case operations; specialist staff join when your Performance Notification requires it.

Or Shamosh, Founder and CEO, ASA Compliance Group, Amazon account reinstatement specialist

Or Shamosh · Founder & CEO

Why this matters
  • Your case log only gets one chance to stay consistent
  • Every submission is compared against what already exists
  • Wrong moves slow reinstatement or shut it down entirely
  • Expert judgment before anything is submitted
Michael Gourin, Chief Commercial Officer, ASA Compliance Group
Executive leadership

Michael Gourin

Chief Commercial Officer

Product, marketing, partner channels, case intake & service structure

Owns product positioning, marketing, partner channels, and intake so sellers enter the right service path with clear scope and the right facts.

Smadar Popovski, Chief Operating Officer, ASA Compliance Group
Executive leadership

Smadar Popovski

Chief Operating Officer

Appeal execution, Seller Central operations & case sequencing

Runs Performance Notification review, POA execution, Seller Central follow-ups, and escalations with disciplined sequencing.

Ready to reinstate your account with confidence? Get my case strategy

Let's see what it will take to resolve this.

Why we ask: tell us what happened. A real person reviews what you send and replies in writing with your case strategy, including our assessment of the case and the approach we recommend. We also include the fee before you decide whether to proceed.

About 3 minutes. We save your progress as you go.

Start with your notice

The claims Amazon commonly flags

These are patterns rather than a blacklist. Whether any of them is a problem depends on the product and the whole presentation.

Treatment or prevention of disease

The clearest category. Language saying the product treats, cures, prevents or mitigates a named condition. Naming the condition is not required: describing its symptoms often carries the same meaning.

This is also where a defence is most likely to be legitimate rather than a retreat. If the product is genuinely regulated and authorised for that use, the answer is the status evidence, and the issue becomes FDA compliance.

Diagnostic language

The product detects, measures, screens for or indicates a condition. Measurement claims are particularly easy to make accidentally on devices that produce a number, because a number invites a clinical reading.

Pain, infection, inflammation or healing

The most common wording on ordinary consumer goods, and the most often assumed harmless. Supports, textiles, topicals and devices routinely carry relief, healing or antibacterial language written as marketing rather than as a claim.

Antimicrobial language deserves separate care: depending on the product and the target it can also raise a pesticide question, which is a different regulator and a different evidence set.

Structure or function of the body

The product changes how part of the body works. Metabolism, appetite, digestion, circulation, approach, sleep. This category is genuinely jurisdiction-dependent, and a claim permitted in one marketplace can be unauthorised in another under a register of approved wording.

Scientific support
Evidence that something is true. Necessary often, and not the same as permission.
Regulatory permission
Whether that wording may be used for that product in that marketplace. This is what a notice is usually about.

Images and enhanced content

Before-and-after photographs, body diagrams, clinical-style graphics, condition references, testimonials and comparison charts. An image can communicate a medical purpose entirely without text, and it survives every edit made to the written copy.

This is the single most common reason a corrected listing gets rejected again. The title is neutral, the enhanced content is not, and nobody looked.

Full-service appeal handling

You send the notice. We handle the case.

AmazonSellersAppeal by Or Shamosh reviews your medical claims notice and evidence, then manages your case in Seller Central.

  1. 01

    Review the notice and history

    We review the notice and identify the wording, images or packaging that led Amazon to flag a medical claim.

  2. 02

    Build the evidence and appeal

    We check the product status and all relevant claims, then prepare supported corrections or an evidence-based response.

  3. 03

    Submit and follow through

    We coordinate the listing response, verify the relevant changes and manage Seller Central submissions, revisions and follow-ups.

Strategy, evidence, appeal writing, submissions and unlimited follow-ups and revisions within the agreed case scope.

Experience behind your appeal

Proof & results

Amazon seller enforcement is our daily work. Amazon Sellers Appeal has handled account, listing and compliance cases across global marketplaces.

Or Shamosh speaking to an audience at the European Seller Conference in Prague
Or Shamosh speaking at the European Seller Conference, Prague, March 2025.
5,500+Cases handled
98%*Historical reinstatement rate
Since 2016Amazon seller appeal specialists
About an hourMost first replies
Full ownershipStrategy, evidence, submissions and follow-ups
Case strategyA written assessment for eligible cases

* Historical results across ASA Compliance Group-managed enforcement cases. Last verified as of .

See more seller results · Watch client videos

Client reviews

What sellers say about Amazon Sellers Appeal

Real names and quotes from clients we’ve helped through reinstatement. Every case has its own timeline and details.

See all reviews

Evidence

Real sellers. Real reinstatements. Each case required a different approach.

Six short videos from sellers who worked with ASA Compliance Group through reinstatement. Every case has its own timeline and details.

Maia“After four months deactivated on a variation issue, others said they couldn’t help. Or got my business, and my dreams, back.”

Nasir“Five years using Or. Very professional and quick on listings, account issues, and safety concerns.”

Nimrod“Sharp, smart, and reliable. If you’re thinking about working with him, you should go for it.”

Eliran“He gives you honest odds upfront, straight with you, even when it’s not what you wanted to hear.”

Fozia“Eight years selling on Amazon. Or fixed every issue. Calm when I was panicking, always a successful outcome.”

Paul“Shut down overnight. Months with another expert failed. Or got us back in the UK and Europe. Or is your man.”

6 client video stories

Watch all client videos

When you’re ready, get your case strategy below. We’ll tell you if we’re the right fit.

Knowledge

How words and images change Amazon's classification

ASA Compliance Group operates Amazon Sellers Appeal. On claims files we inventory every surface, then correct what moved the classification or document the product status that permits it, and verify the live result.

Medical-claims enforcement is about intended use rather than the presence of health-related words. A claim that a product diagnoses, treats, cures, mitigates or prevents disease, or affects the structure or function of the body, can move an otherwise ordinary product into a regulated category.

That is why a keyword list is the wrong tool and this page does not publish one. The same word can be unremarkable on one product and controlling on another, because what matters is the purpose the whole presentation communicates: the surrounding text, the imagery, the product type, the audience and the implied promise.

Three things the notice may be asking for, and they are not the same request:

Remove the claims

The product is fine and its description is not. A complete, verified correction across every surface is the answer.

Prove the status

The product may genuinely be regulated. Then the answer is the classification evidence, not a denial that it is medical.

Both

Common. Inaccurate claims corrected, and the legitimate regulated status evidenced, without conceding either point wrongly.

One boundary worth stating early: a listing-level removal is not an account suspension, and the two are routinely confused in the same message. Amazon's disclosure and claim restrictions govern the marketplace side. FDA's own material on structure and function claims and cosmetic labelling claims explains where the regulatory line sits, and it is jurisdiction-specific. Where the outcome is that the product itself becomes ineligible, the issue is restricted products; where the case turns on the product's safety documentation rather than on the wording of the claim, product safety compliance is the issue, and testing alone never authorises a medical, disease or treatment claim: that turns on lawful classification, an authorised intended use and permitted wording; and the catalog half of any correction is incorrect detail page.

Appeals

Why DIY medical-claims appeals get rejected

Reviewers check whether the medical purpose is still being communicated anywhere. Most rejected responses corrected the place it was easiest to see.

One surface corrected

The phrase removed from the title while equivalent meaning stays in bullets, images, enhanced content, video or backend terms.

Pointing at competitors

Others use the same words. That establishes nothing about this listing, and reviewers are looking at this one.

Blaming the manufacturer

The copy came from the brand. The seller remains responsible for content it contributes or adopts.

Studies instead of permission

General scientific literature offered where the question is whether that wording is permitted for that product in that marketplace.

Denying while the label says otherwise

The product called non-medical while its packaging, instructions or historical content describe medical use.

The claim comes back

Prohibited wording re-uploaded through a feed, enhanced content, advertising or external synchronisation after the appeal was filed.

Your evidence, explained

Amazon medical claims appeal: evidence checklist

A focused appeal connects your notice with verifiable records. Here is what we review: listing wording, product images, labels and supporting product records.

Diagnosis

Start from the notice and identify the flagged claim if it names one. Often it does not, and the work is to find the strongest likely trigger from the full historical capture. Content that has since been edited can still be what drove the classification, so the history matters as much as the current page.

Then establish what the product actually is and does, from the physical packaging, the label, the instructions, any insert and the manufacturer's own intended-use material. This decides whether the route is correction or classification evidence, and guessing it is how files go in the wrong direction for weeks.

The surface inventory

Every place a medical purpose can be communicated, current and historical, each marked correct, to be corrected, or defensible:

  • Title, bullets and description
  • Images, including any text inside them
  • Enhanced brand content and video
  • Backend search terms, product type and browse node
  • Advertising copy and targeting
  • Packaging, inserts and instructions
  • External sites synchronising content in

The last two are outside the catalog and inside the problem. A physical insert making the claim is not fixed by any amount of catalog work.

Correction, or defence

Where the claims are inaccurate or unpermitted, correct them everywhere and keep the evidence of each removal. Where the product is genuinely regulated and authorised, the response should say so and prove it rather than denying the medical character, because a denial that the evidence contradicts damages the rest of the file.

Where a claim is defensible under a marketplace-specific authorised register, the wording usually has to match closely rather than approximately. A permitted claim rephrased for marketing is often no longer the permitted claim.

Where the exact claim is defensible because the product is lawfully classified or authorised for that intended use and the wording is permitted, the regulatory-status route carries it. Safety testing alone does not authorise a disease, treatment or medical-purpose claim. A test report answers whether the product is safe. It does not answer whether the sentence on the listing is one you are allowed to write.

Verification, surface by surface

Catalog work runs through prepared, uploaded, processed and live-verified, and each surface is checked on its own. A processing report saying rows were accepted says nothing about enhanced content or images.

Add the control that stops recurrence: who may write product copy, what patterns are prohibited, what gate approves a claim before publication, and where that record is kept. Feeds and external synchronisation need to be inside that gate, because they are the usual route back in.

Have ready when you submit intake

  • The exact notice text and the flagged claim if named
  • What the product is and what it actually does
  • Photographs of packaging, inserts and instructions
  • Current and historical listing content, all surfaces
  • Any regulatory status or authorised-claim basis
  • Feeds or external sources that write to the listing
  • Every prior appeal, case and Amazon reply

If enhanced content or video was created by someone else and cannot be edited quickly, say so. It changes the sequencing rather than the outcome, and it is better known at the start.

Amazon medical claims appeal FAQs

For sellers who already have the Performance Notification. Broader questions: full FAQ library.

Which words usually trigger a medical-claims review?
The useful focus is claim meaning rather than a list of words. Language about diagnosing, treating, curing, mitigating or preventing disease, or changing the structure or function of the body, can create risk depending on context. Review the surrounding text, the images, the product type, the audience and the implied promise across every catalog and physical surface.
Can images or enhanced content trigger the violation?
Yes, and they often are the trigger. Before-and-after images, body diagrams, condition references, clinical-style graphics, testimonials, comparison charts, enhanced modules and video can communicate a medical intended use even where the title is entirely neutral. Capture current and historical content, correct every surface, and verify what is actually live after processing.
What if the manufacturer makes the same claims?
That does not by itself make the claim acceptable on Amazon or appropriate for the product's regulatory status. Verify the claim, the intended use, any supporting authorisation, the physical label, the marketplace and the applicable policy. The seller remains responsible for the content it contributes or adopts and for representing the product accurately.
Is removing the claim enough?
Sometimes a complete and verified listing correction is the whole answer. It is not enough where the physical label makes the same claim, the product is genuinely regulated, old inventory remains, or Amazon asked for documentation rather than removal. Keep prepared, uploaded, processed and live-verified as separate states in any response.
What if the product really is a regulated device?
Then confirm the exact classification, the intended use, the manufacturer and model, the official listing or authorisation, the labelling and the seller-to-manufacturer relationship, and map each record to the listing. Correct inaccurate claims without denying a legitimate regulated status that the evidence supports, because being regulated is not itself the violation.
What do you need to start?
The notice text and the flagged claim if it names one, what the product actually does, photographs of packaging and instructions, the listing content across every surface, and every prior appeal or Amazon reply.
What is in the Case Strategy?
Your Case Strategy sets out our assessment of the notice, the evidence needed, the appeal approach and the next steps for your seller account or ASINs. We focus on listing wording, product images, labels and supporting product records. You receive a clear plan for preparing the response and managing the case.

Your case stays with one team for the evidence review, appeal, submissions and follow-ups.

Start here

Get a strategy for your medical claims appeal

Include the flagged wording if it is named, what the product actually does, and the packaging and instructions. Four short steps. Or Shamosh reads every intake.

  • Every case is personally reviewed before we take it on.
  • Most first replies are sent within about an hour.
  • Eligible cases get a written Case Strategy tied to your Performance Notification.
Or Shamosh, Founder and CEO, ASA Compliance Group

Or Shamosh · Founder and lead strategist

5,500+ enforcement cases since 2016. Every intake is personally assessed before acceptance.

Send what you have, including prior DIY or agency appeals. We say what is viable in writing before you commit.

Questionnaire

If the questionnaire does not load, open intake on the account page.

What happens after you submit

  • You’ll receive a review email within about one hour.
  • If Amazon gave you a reply deadline, mention it in the form so we can time delivery to it.
  • If eligible, you receive a written Case Strategy: what is driving the enforcement, what we would argue, what evidence matters, and how we would run Seller Central.

Send the notice. Get the strategy.

If Amazon removed a listing over medical or health claims, start with the questionnaire.

For individual ASIN issues, explore listing reinstatement. For a different notice, browse all suspension types.