Egyptian Drug Authority · Egypt
DEA-EG-2025-0065
Tier 1 · Regulator-publishedClass IIIRecolhaStatus · active
- Issuing authority
- Egyptian Drug Authority (EDA)
- Authority reference
- periodic report no(65) For 2025
- Date issued
- Sept 2025
- Recorded by us
- 2026-09-06 19:45:29 UTC
- Produto
- hypodermic syringe with safety needle
- 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
- Not stated by the issuing authority
- Manufacturer country
- Not stated by the issuing authority
- MAH or importer
- Not stated by the issuing authority
- Números de lote
- 2501
- Prazos de validade
- Not published with the notice
- Action type
- Recolha
- Classificação
- Class III as issued
- Indicative severity
- Not assessed by Drug Eye Africa
- Defect category
- Falsificado
- Product type
- Not stated by the issuing authority
- ATC code
- Not stated by the issuing authority
- Affected markets
- Egypt — no market beyond the issuing country was named on the notice
- Cross-border event
- Not linked to a cross-border event
- Texto do aviso
- hypodermic syringe with safety needle
1ml size
2501
01/2025تاريخ انتاج
12/2029تاريخ انتهاء
غير مدونرقم التسجيل
الدولية للمستلزمات الطبيةالشركة المصنعة
وذلك بناءً على ماورد الينا من إدارة التفتيش على
مصانع المستلزمات ، حيث افادت بان المستلزم الذى
يحمل البيانات الموضحة اعلاه هو مجهول المصدرو
غير مدون عليه رقم تسجيل
سحب ووقف تداول وتحريز
في حالة الشك في المستحضر الصيدلى يتم
الرجوع إلى هيئة الدواء المصرية سواء
بالإتصال بالخط الساخن 15301او الموقع
الإلكترونى الخاص بالهيئة.
سبتمبر 2025
اسم المستلزم
رقم التشغيلة
سبب التحذير
الإجراءات
التصحيحية
نصائح
للمستهلكين
منشور
سحب
هذا التنبية خاص بالتشغيلات الواردة في المنشور فقط ولا
ينطبق على تداول المستحضر بشكل عامOriginal language: ar
- Texto do aviso em inglês
- Notice. Hypodermic syringe with safety needle, 1ml size, batch 2501, manufactured 01/2025, expiry 12/2029, registration number not printed, manufactured by the International Company for Medical Supplies. Issued on the basis of what the department reported to the Authority.Machine translation, produced by Drug Eye Africa and not checked by the issuing authority. The authority stated only the text above it.
- Estado
- Em vigor
- Superseded by
- Not superseded. This is the current version.
- Version
- 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
- 78b905dd4ff84d5b8bdeccb93bd918d2c147ba2c27c688e682484c5e6bbe6240SHA-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 20:47:13 UTC
| Reference | Date | Country | Product | Batches | Action | Class | Source |
|---|---|---|---|---|---|---|---|
| DEA-XXX-2026-0003 | 03 Jul 2026 | XX | DARZALEX (daratumumab) | MYS7381 · STV1K01 | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-EG-2026-0070 | Jul 2026 | EG | Tagrisso 80 mg film-coated tablets | FEST | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-XXX-2026-0002 | 16 Jun 2026 | XX | JAKAVI (ruxolitinib) | none published | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-EG-2026-0062 | Jun 2026 | EG | COLOVERIN-D 30 film Coated Tablets | 251035A | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-EG-2026-0061 | Jun 2026 | EG | FLOPADEX 8mg Hard gelatin capsules 30 | 2504626 | Public warning | Unclassified | Tier 1 · Regulator-published |
| DEA-EG-2026-0060 | Jun 2026 | EG | Tears Guard Artificial Tears & Lubricant (Sterile Ophthalmic Solution) | 0425118 | Public warning | Unclassified | Tier 1 · Regulator-published |
Cite this record
Drug Eye Africa (2025). DEA-EG-2025-0065: hypodermic syringe with safety needle — Recolha, Egyptian Drug Authority. Register of African Regulatory Actions. https://drugeyeafrica.org/register/notice/eg/2025/dea-eg-2025-0065Version history
v1Manufacturer removed: the notice describes packs of unknown origin (correction)
—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.