| Input | Your submission |
|---|---|
| Platform / marketplace | Amazon.de (also selling .fr and .it) |
| Error code or current status | Error 5995 on bulk upload; individual ASINs show “Your submission is under review” |
| SKU count affected | 34 SKUs, 6 product types |
| Already submitted | Suppliers' CE test reports + the supplier's own Declaration of Conformity (PDF, in the supplier's name) |
| Responsible Person appointed | Yes — a German forwarding address bought through a service, named on the product label |
| Duration stuck | 5 weeks, 3 resubmissions |
This is the reason nothing you submit is moving. Error 5995 is not a document-validation error — it is a permission error. Amazon restricts bulk safety and manufacturer edits to the account holding the registered Brand Owner role for that ASIN. Your account is a reseller on these ASINs, so the bulk path is closed to you regardless of how good the documents are.
The reason you also see “under review” and not a clean rejection is that your resubmissions are going in through a route that queues the file but can never satisfy the brand-role check. That is what produces the loop other sellers describe as “submit, wait 7 days, back to required”.
You are submitting the supplier's DoC. But your own brand is on the product, which makes you the manufacturer for the purposes of the declaration — so a DoC that does not name you does not satisfy the check, even though it is a genuine, valid document.
The supplier's safety forms are not evidence for your listing. What is being checked is whether the responsible economic operator chain is clearly defined and named by you.
A purchased forwarding address is frequently insufficient. The named person must be an EU-established economic operator who accepts the legal responsibility, with a physical address and contact details a consumer can actually reach — and those details must appear on the product, its packaging, or an accompanying document.
I checked the labs named on the report you supplied against Amazon's Suspended Validation Labs list. Neither appears on it. Your test reports are usable — keep them, you will need them in step 3 below.
Do these in order. Steps 1 and 2 are the ones that unblock you; step 3 makes the file pass once you are through.
MYC is per-ASIN and will time out if you try all thirty-four. Work in batches of five, submit, note the date, and wait for a status change before moving on. Record each batch in a sheet with: ASIN, date submitted, status, days elapsed. You will need this if you have to escalate.
File these three, in this order, for each ASIN. Use the versions below, adapted to your company details.
This is a self-declaration — no lab and no consultant has to sign it. It must name you as the manufacturer and be based on the test reports you already hold.
EU DECLARATION OF CONFORMITY
1. Product / model: [PRODUCT TYPE], model [MODEL NUMBER]
Batch / serial identifier: [BATCH OR SERIAL]
2. Name and address of manufacturer:
[YOUR COMPANY LEGAL NAME]
[FULL POSTAL ADDRESS]
[COUNTRY] — [CONTACT EMAIL]
3. This declaration of conformity is issued under the sole responsibility
of the manufacturer.
4. Object of the declaration:
[DESCRIPTION: what the product is, what it is used for, how it is used]
5. The object of the declaration described above is in conformity with the
relevant Union harmonisation legislation:
- Regulation (EU) 2023/988 General Product Safety Regulation
- [ADD APPLICABLE, e.g. Directive 2014/30/EU (EMC), 2011/65/EU (RoHS),
Regulation (EU) 2023/1542 (batteries) — only those that apply]
6. References to the relevant standards used:
- [EN STANDARD] e.g. EN 55032 / EN 55035 (EMC)
- [EN STANDARD]
(Taken from the test reports on file for the model above.)
7. Name and address of the person authorised to compile the technical file /
EU responsible person:
[RESPONSIBLE PERSON LEGAL NAME]
[EU PHYSICAL ADDRESS]
[CONSUMER-REACHABLE EMAIL]
8. Signed for and on behalf of: [YOUR COMPANY LEGAL NAME]
Place and date of issue: [CITY], [DATE]
Name, function, signature: [NAME], [ROLE]
This is the document most sellers never produce, and its absence is why files pass format checks and still fail. It does not need to be long. For each product type answer the hazard questions honestly and state what you did about each:
| Hazard area | Your product | Measure taken |
|---|---|---|
| Electrical safety / heat | Mains-connected, LED driver | Test report [REF] to EN 55032/55035; CE-marked driver; thermal cut-out |
| Materials in contact with user | ABS housing, no skin contact beyond handling | RoHS declaration [REF]; REACH compliance statement from supplier |
| Small parts / entrapment | No detachable parts under 3 cm | Assembly fixed; pull test [REF] |
| Ingress / liquids | Indoor dry use only | IP rating declared: IP20; warning in label text |
| Battery | None | Not applicable |
| Misuse / foreseeable wrong use | Covered outdoor or with damaged cable | Warning statements below; instruction sheet |
| Vulnerable users / children appeal | Not child-directed | Warning statement; no decorative food-like appearance |
| Residual risk | Low — all identified hazards mitigated by the measures above, verified by [TEST REFS] | |
[MANUFACTURER LEGAL NAME]
[FULL POSTAL ADDRESS]
[CONTACT EMAIL]
EU RESPONSIBLE PERSON: [LEGAL NAME], [EU ADDRESS], [EMAIL]
EN WARNING: For indoor use only. Do not use with a damaged cable
or plug. Do not cover. Not a toy — keep away from children.
DE WARNUNG: Nur für den Innenbereich. Nicht mit beschädigtem Kabel
oder Stecker verwenden. Nicht abdecken. Kein Spielzeug —
von Kindern fernhalten.
FR AVERTISSEMENT: Usage intérieur uniquement. Ne pas utiliser avec un
câble ou une fiche endommagé(s). Ne pas couvrir. Ne pas laisser
à la portée des enfants.
Model / Modell / Modèle: [MODEL]
Batch / Charge / Lot: [BATCH]
EAN: [EAN]
Warning text must appear in the official language of each country of sale. Because you sell in .de, .fr and .it, all three are required for those marketplaces — a single English block is not sufficient. Add the Italian block before you file for .it.
Only use this after Step 1 and 2 are done and a submission has been in review for more than 7 days. Paste as-is, filling the brackets. It gives support a specific technical finding rather than a complaint, which is what moves cases out of the loop.
Subject: GPSR submission blocked by brand-role permission error — case set [BATCH REFERENCE] I am submitting GPSR compliance information for [N] ASINs via Manage Your Compliance (Product Compliance Requests) on seller account [SELLER ID]. Attempting a catalogue update returns Error 5995. I understand this error relates to brand-name permissions and that my account is not the registered Brand Owner on these ASINs. I am therefore filing at SKU level through MYC, not via a catalogue push. Submissions for the following ASINs have been in "under review" status for [D] days, with no change and no rejection reason provided: [LIST ASINs AND SUBMISSION DATES] For each ASIN I have provided: 1. EU Declaration of Conformity in my name as manufacturer 2. Internal risk analysis under Article 9.2.a 3. Test reports from [LAB NAME], not on the Suspended Validation Labs list 4. EU Responsible Person declaration: [RP LEGAL NAME], [EU ADDRESS] Please confirm either (a) which specific document is deficient and why, or (b) that the submissions meet requirements and will be processed. I have held stock in FBA for these ASINs since [DATE]. Please treat this as time-sensitive. [YOUR NAME] — [SELLER ID] — [EMAIL]
Sellers report roughly 30 days from deactivation before FBA stock is scheduled for automatic destruction. Working from your deactivation date:
| Milestone | Date (from your case) | Action |
|---|---|---|
| Deactivation | Day 0 | Stop resubmitting the old file set |
| Step 1 & 2 complete | Days 1–3 | File all ASINs through MYC in batches of 5 |
| First status check | Day 10 | If still “under review” and no reason given, send the escalation script |
| Decide on removal order | Day 18 | If still unresolved, request a removal order rather than lose the stock |
| Destruction risk window | Day 30 | Hard deadline |
This is the report you get for your own case.
Blocker classification, fix sequence, corrected documents, escalation script and stock countdown — 24 hours after you send me your error message.
Get my diagnosis — €12