Rwanda Food and Drugs Authority · Rwanda
DEA-RW-0000-37309172
Tier 1 · Regulator-publishedClass IRecolhaStatus · active
- Issuing authority
- Rwanda Food and Drugs Authority (RWANDAFDA)
- Authority reference
- Not stated by the issuing authority
- Date issued
- 11 Oct 2019Ambiguous date in the source: could be 2019-10-11 or 2019-11-10. The column is descending, and that does not decide between them. Left unresolved.
- Recorded by us
- 2026-09-06 18:40:27 UTC
- Produto
- Ranitidine ( all Brand ,all batches)
- INN / active substance
- Not stated by the issuing authority
- Dosage form
- Not stated by the issuing authority
- Strength
- Not stated by the issuing authority
- Fabricante
- all
- Manufacturer country
- Not stated by the issuing authority
- MAH or importer
- Not stated by the issuing authority
- Números de lote
- Not published with the notice
- Prazos de validade
- Not published with the notice
- Action type
- Recolha
- Classificação
- Class I as issued
- Indicative severity
- Not assessed by Drug Eye Africa
- Defect category
- Impureza
- Product type
- Medicamento
- ATC code
- Not stated by the issuing authority
- Affected markets
- Rwanda — no market beyond the issuing country was named on the notice
- Cross-border event
- Not linked to a cross-border event
- Texto do aviso
- contain nitrosamine impurity classified as probable human carcinogenOriginal language: en
- Estado
- Em vigor
- Superseded by
- Not superseded. This is the current version.
- Version
- 13
Where this record came from, and what is held to show it.
- Primary source
- https://monitoring.rwandafda.gov.rw/recalls/
- Copy of the source
- Taken and held by Drug Eye Africa, so the record survives the link above being moved or withdrawn. Not yet published at an address you can open.Ask us for it and check it against the fingerprint below.
- Fingerprint
- 60f6d564c1222b3b6ec906daff230258c238d352b147c51672d47f194babea72SHA-256 of the copy held. Any file that produces this number is that copy, byte for byte; any file that does not is a different document.
- Copy taken
- 2026-09-11 09:58:19 UTC
| Reference | Date | Country | Product | Batches | Action | Class | Source |
|---|---|---|---|---|---|---|---|
| DEA-RW-0000-86468251 | 07 Oct 2021 | RW | Losar-Denk 50 mg film Coated DENK PHARMA | none published | Recall | Class I | Tier 1 · Regulator-published |
| DEA-RW-0000-51547910 | 07 Oct 2021 | RW | Losar-Denk 25 mg film Coated DENK PHARMA | none published | Recall | Class I | Tier 1 · Regulator-published |
| DEA-RW-0000-40943378 | 07 Oct 2021 | RW | Colosar-Denk 100 mg /12,5mg film coated tablet DENK PHARMA | none published | Recall | Class I | Tier 1 · Regulator-published |
| DEA-RW-0000-25020792 | 07 Oct 2021 | RW | Losar-Denk 100 mg film Coated DENK PHARMA | none published | Recall | Class I | Tier 1 · Regulator-published |
| DEA-RW-0000-16076249 | 07 Oct 2021 | RW | Colosar-Denk 50mg /12,5mg film coated tablet DENK PHARMA | none published | Recall | Class I | Tier 1 · Regulator-published |
| DEA-UG-2019-36916109 | 31 Oct 2019 | UG | Ranitidine | none published | Import hold | Unclassified | Tier 1 · Regulator-published |
Cite this record
Drug Eye Africa (2019). DEA-RW-0000-37309172: Ranitidine ( all Brand ,all batches) — Recolha, Rwanda Food and Drugs Authority. Register of African Regulatory Actions. https://drugeyeafrica.org/register/notice/rw/2019/dea-rw-0000-37309172Version history
—No version history recorded for this record.
—Corrections appear here and in the site-wide log. Records are superseded, never deleted.
Verification
Tier 1 — Published by the issuing regulator on its own channel and captured by Drug Eye Africa, with the source document archived.
Indexing
This record is indexable: it is dated, names a product, and carries either a batch number or a stated reason.