RECORDS ARE PUBLISHED REGULATORY ACTIONS. FIELDS THE ISSUING AUTHORITY DID NOT PUBLISH ARE MARKED AS NOT STATED, NEVER FILLED IN.
Drug Eye AfricaNational Actions, Continental Reach
Register / Rwanda / DEA-RW-0000-86468251
Rwanda Food and Drugs Authority · Rwanda
DEA-RW-0000-86468251
Tier 1 · Regulator-publishedClass IRecallStatus · activeNot shown in search engines
Issuing authority
Rwanda Food and Drugs Authority (RWANDAFDA)
Authority reference
Not stated by the issuing authority
Date issued
Not dated on the authority's listingAmbiguous date in the source: could be 2021-10-07 or 2021-07-10. The column is descending, and that does not decide between them. Left unresolved.
Recorded by us
2026-09-06 18:40:27 UTC
Product
Losar-Denk 50 mg film Coated
INN / active substance
Not stated by the issuing authority
Dosage form
Not stated by the issuing authority
Strength
Not stated by the issuing authority
Manufacturer
DENK PHARMA
Manufacturer country
Not stated by the issuing authority
MAH or importer
Not stated by the issuing authority
Batch numbers
Not published with the notice
Expiry dates
Not published with the notice
Action type
Recall
Classification
Class I as issued
Indicative severity
Not assessed by Drug Eye Africa
Defect category
Impurity
Product type
Medicine
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
Notice text
Genotoxic impurity detected in API
Original language: en
Status
Active
Superseded by
Not superseded. This is the current version.
Version
5

Provenance

Verification tier 1

Where this record came from, and what is held to show it.

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Taken and held by Drug Eye Africa, so the record survives the link above being moved or withdrawn.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
59b5df2a915961d640cf3bc473e9d7b9830b37b39d3b5573d2730905fba91d45
SHA-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
2026-09-08 12:29:55 UTC

Related actions elsewhere

Same stated defect
ReferenceDateCtryProductBatchesActionClassSource
DEA-RW-2024-8123105812 Apr 2024RWBenylin Pediatrics Syrup BN:329304, Mfd: May 2021,Exp:April 2024
Johnson & Johnson, South Africa
329304RecallClass ITier 1 · Regulator-published
DEA-RW-2019-7422246918 Jun 2019RWBiperiden.HCl Sterop Tablets 2 mg
Lab. STEROP NV, Belgium
18B05RecallClass ITier 1 · Regulator-published
DEA-RW-2019-5743294418 Jun 2019RWChloramphenicol 0.5% w/v Eye Drops B.P;
Abacus Parenteral Drugs Ltd., Uganda
131936RecallClass IITier 1 · Regulator-published
DEA-RW-0000-51547910undatedRWLosar-Denk 25 mg film Coated
DENK PHARMA
none publishedRecallClass ITier 1 · Regulator-published
DEA-RW-0000-40943378undatedRWColosar-Denk 100 mg /12,5mg film coated tablet
DENK PHARMA
none publishedRecallClass ITier 1 · Regulator-published
Cite this record
Drug Eye Africa (0000). DEA-RW-0000-86468251: Losar-Denk 50 mg film Coated — Recall, Rwanda Food and Drugs Authority. Register of African Regulatory Actions. https://drugeyeafrica.org/register/notice/rw/0000/dea-rw-0000-86468251

Version history

No version history recorded for this record.
Corrections appear here and in the site-wide log. Records are superseded, never deleted.

Verification

Tier 1Published by the issuing regulator on its own channel and captured by Drug Eye Africa, with the source document archived.

Indexing

This record is kept out of search engines, because the issuing authority did not state a date. That lasts until the missing part is filled in. The record is held here in full in the meantime, and is found by searching this site.