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 / South Africa / DEA-ZA-2022-88598902
South African Health Products Regulatory Authority · South Africa
DEA-ZA-2022-88598902
Tier 1 · Regulator-publishedUnclassifiedRecallStatus · active
Issuing authority
South African Health Products Regulatory Authority (SAHPRA)
Authority reference
Not stated by the issuing authority
Date issued
17 Oct 2022SAHPRA heads this column "Date Updated" rather than the date of the recall.
Recorded by us
2026-09-06 20:25:58 UTC
Product
Lasix 80 mg tablets (furosemide 80 mg)
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
Not stated by the issuing authority
Manufacturer country
Not stated by the issuing authority
MAH or importer
Not stated by the issuing authority
Batch numbers
CG022A
Expiry dates
Not published with the notice
Action type
Recall
Classification
Not stated by the issuing authority
Indicative severity
Not assessed by Drug Eye Africa
Defect category
Not stated by the issuing authority
Product type
Not stated by the issuing authority
ATC code
Not stated by the issuing authority
Affected markets
South Africa — no market beyond the issuing country was named on the notice
Cross-border event
Not linked to a cross-border event
Notice text
Not captured. The notice itself is linked below.
Status
Active
Superseded by
Not superseded. This is the current version.
Version
3

Provenance

Verification tier 1

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

Primary source
https://www.sahpra.org.za/document/lasix-80-mg-tablets-furosemide-80-mg/
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Taken and held by Drug Eye Africa, so the record survives the link above being moved or withdrawn.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
e812f3b76022a809e3a39eb09ab310b7d0211dcbec75d6c0a306808ebf06fea4
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
2026-09-06 20:52:42 UTC
Cite this record
Drug Eye Africa (2022). DEA-ZA-2022-88598902: Lasix 80 mg tablets (furosemide 80 mg) — Recall, South African Health Products Regulatory Authority. Register of African Regulatory Actions. https://drugeyeafrica.org/register/notice/za/2022/dea-za-2022-88598902

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 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.

This record as data

/api/v1/notices/DEA-ZA-2022-88598902