Direct answer: classify the product and event first. Then build or review the China safety file, preserve evidence, assess corrective action, and coordinate the relevant regulatory, consumer, civil, insurance and communications tracks. Product-specific rules and incident facts control. This is orientation — not legal, technical, medical or recall advice.
Related: Consumer protection · GT vs CBEC · 12315 SOP · Life sciences hub · Personal injury · Contracts · Trade & customs.
Direct answer
Classify before anyone decides this is a recall or a liability case.
- What product, China sales/import route and actor are involved? Consumer good, vehicle, device, food, drug or industrial — plus GT, CBEC, OEM or platform.
- Which standards, certification, registration, labeling and safety rules apply? Mandatory GB vs GB/T; CCC or sector approval; Chinese warnings.
- What is the incident status? Quality/warranty, safety signal, suspected defect, injury, regulator inquiry, recall or claim — they are not the same track.
- What evidence must be preserved and what technical question needs testing? The incident unit, batch/serial, labels, QC and a posed appraisal question.
- Which containment, corrective, regulator, consumer, insurance and comms tracks must run together?
- Which specialist is needed by sector, authority, testing issue and urgency?
The spine remains Risk → Evidence → Claims → Resolve. This page turns it into a safety file, hold, defect/actor screen, sector recall router and counsel brief.
Orientation and screening only. Not legal, technical, medical or recall advice. Do not universalize consumer-product working-day figures onto vehicles, devices, drugs or food. Chinese official texts and product-specific rules control.
PQLSAMR recallSectorConsumerCCC / GBPractice
- Classify product, market route, actor and incident status before calling it a recall or liability case.
- Consumer goods
- Toys · electronics
- Vehicle
At-a-glance situation table
| Situation | First question | Core module | First output |
|---|---|---|---|
| Pre-market launch | Can this product be lawfully and safely placed on the China market? | Safety file | Standards / cert / label / traceability checklist |
| Recurring complaints | Isolated issue or a systemic safety signal? | Incident classifier | Escalation tier + evidence hold |
| Serious injury / death | What must be contained, preserved and reported now? | Incident command | Immediate action matrix |
| Regulator sampling / inquiry | Which authority, scope and records? | Inspection protocol | Fact / evidence + comms brief |
| Suspected recall | Which product-specific regime applies? | Sector recall router | Timeline only after classification |
| Consumer claim | Quality, defect/tort, consumer right, or all three? | Defect / actor desk | Claim + defense + evidence map |
| Supplier / OEM defect | Public-facing duty versus contractual recourse? | Supply-chain protocol | Technical + indemnity / insurance stream |
| CBEC / platform issue | Which sales / fulfilment / import model is actually used? | GT vs CBEC matrix | Actor / label / after-sales map |
Scope: keep the legal tracks separate
- Safety/compliance, quality/warranty, defect/tort, consumer, recall and criminal escalation.
- Safety /
- Can it be sold?
- Standards / CCC
- Cite article + product scope + effective date. Last checked 13 August 2026.
- Product Quality Law, Civil Code tort, consumer law, SAMR recall rules, vehicle and sector regimes.
- Product Quality Law — quality, seller duties, defect liability, supervision
- Civil Code tort + Consumer Law
- Injury / after-sales / ads
Law · Product Quality Law Arts. 26–27 (quality / identification / warnings). Unreasonable danger, standards conformity, represented quality, and Chinese identification/warnings. Cite the precise article for the claim. Chinese text controls.
Law · Product Quality Law Arts. 33–40 and 41–46. Seller incoming-inspection and quality-remedy concepts (33–40). Producer/seller defect paths, defenses/recourse, defect concept and limitation framework (41–46). Last checked 13 August 2026.
SAMR · Interim Provisions on Consumer Product Recall (in force 1 Jan 2020). Applies to covered consumer products after classification. Serious-defect / foreign-recall information: report to the provincial market regulator within 2 working days of discovery (Art. 8 style trigger). Plan, public notice and close-out clocks are branched — not one generic date. Vehicles, devices, drugs and food have other rules. Last checked 13 August 2026.
China product safety file
Mandatory standards and certification (CCC where applicable) shape both compliance and later liability narratives. They do not, by themselves, decide causation.
- Ten-element pre-market safety file from classification through insurance and incident plan.
- 1. Product class + intended use
- 2. GB vs GB/T / sector rules
- 3. CCC / registration / filing
Actor and responsibility desk
Consumers may pursue sellers and manufacturers; supply-chain contracts then allocate indemnity. Platforms can be pulled in when seller identity is unclear or statutory platform duties are unmet.
- Producer, seller, importer, brand, platform and OEM have different public-facing and contract roles.
- Design / make /
- label / release
- Incoming inspect
Defect theories and causation evidence
Claims may allege manufacturing defects, design defects, or inadequate warnings/instructions. For foreign designs localized for China, Chinese-language warnings are a frequent battleground. Judicial appraisal often drives causation.
- Test the right configuration. Do not destroy, alter or silently replace the incident unit.
- Compliance evidence versus causation evidence. Injury alone does not prove defect.
- Alleged defect
- Design · make ·
- warning hypothesis
Practical workflow — incident command
- Detect, contain, preserve, assess, correct, notify, close. No duration promise.
- 1. Detect
- One-off or trend?
- Injury / inquiry?
Sector recall router and consumer-product clock
Automobiles and certain consumer products have formal recall regimes. Voluntary remediation can mitigate harm but must stay consistent with regulatory notices — not ad hoc silence.
Do not publish one “China recall timeline.” Route the product first. The working-day figures below apply only after classification confirms the 2020 consumer-product regime and no sector rule supersedes it.
- Life-sciences products use NMPA / MAH playbooks, not toy-recall clocks.
- Route consumer products, vehicles, devices, food, drugs and industrial goods before applying timelines.
- General consumer product
- SAMR 2020 Interim Provisions
- 2-day / plan / public notice
- SAMR Interim Provisions 2020. Only after classification confirms this regime. Not for vehicles, devices, drugs.
- STOP — if vehicle, device, drug, food/cosmetic sector rules apply, do not use these numbers
- Serious info /
- foreign recall
Life sciences: hub · SaMD · device distribution · HGR.
General trade vs CBEC / platforms
CBEC models change importer-of-record and labeling expectations. After-sales promises advertised online can become consumer-law obligations. They do not switch off safety analysis.
- Map the actual fulfilment path. Deep dive: /china-cbec-vs-general-trade-consumer-liability.
- Actor, import, labels, traceability and recall differ by fulfilment model. CBEC is not a liability off-switch.
- Field
- General trade
- CBEC / platform
Supply-chain recourse, insurance and governance
Specs, audit rights, batch traceability, insurance and indemnity help recovery. They do not eliminate consumer-facing exposure. Notify product-liability insurers early and preserve coverage conditions.
- Indemnity runs beside the public duty. Do not backfill records after an inquiry starts.
- Public-facing duty versus contract recovery, insurance notice and communications control.
- Supplier contract
- Spec · audit · CAPA
- samples · cooperate
Regulator sampling and inspection
- Confirm the authority, legal basis, product scope and request immediately.
- Preserve units, labels/manuals, testing, batch/QC, complaint, supplier and distribution records.
- Do not alter, recreate or backfill records after learning of the inquiry.
- Separate factual cooperation, legal positions, public communications and insurer notifications.
- Track deadlines, samples taken, copies supplied and follow-up commitments. PQL Arts. 15–18 frame sampling/reinspection powers in general terms.
Common mistakes
| Mistake | Why it is risky | Use this tool |
|---|---|---|
| “We passed CCC / testing, so liability is solved.” | Compliance evidence does not decide every defect/causation question. | Compliance vs causation desk |
| “Every recall follows the same China timeline.” | Categories have different regimes. | Sector recall router |
| “The supplier indemnity shifts the problem away from us.” | Contract recourse does not remove regulatory / consumer / tort duties. | Public duty + recourse matrix |
| “Delete the listing while we investigate.” | Evidence, traceability and duties can be compromised. | Containment + preservation log |
| “A complaint is just customer service.” | Trends can be early safety signals. | Signal dashboard + escalation |
| “CBEC means China product rules never apply.” | Depends on product and the actual import/seller model. | GT vs CBEC classifier |
Action checklist
Pre-market safety file
- [ ] Classify product and intended use.
- [ ] Identify China market / import / CBEC route and responsible actors.
- [ ] Map current mandatory and recommended standards and sector rules.
- [ ] Confirm certification / registration / filing needs.
- [ ] Link each test report to product model / version and standard edition.
- [ ] Approve Chinese labels, warnings and manuals.
- [ ] Document supplier / OEM quality controls and change approval.
- [ ] Establish batch / serial traceability and retained-sample process.
- [ ] Create complaint / adverse-event escalation rules.
- [ ] Confirm recall / incident governance and insurance notification contacts.
Incident response
- [ ] Stop and classify the event before calling it a recall.
- [ ] Preserve the incident unit, comparable samples and chain of custody where safe.
- [ ] Issue appropriate records / data holds.
- [ ] Map model / batch / serial and distribution scope.
- [ ] Identify the applicable product-specific regulator / recall rule.
- [ ] Separate the compliance question from the causation question.
- [ ] Coordinate technical, legal, regulatory, insurance and communications streams.
- [ ] Document containment / corrective-action decisions and their factual basis.
- [ ] Track authority / customer / platform communications and deadlines.
- [ ] Close with CAPA, effectiveness review and record retention.
City guides
Local AMR practice and courts vary. Currently covered:
Counsel filters: product category · regulator / recall · appraisal / testing · CBEC · insurance · injury · urgency. Product liability lawyers.






