Egyptian Drug Authority · Egypt
DEA-EG-2026-0033
Tier 1 · Regulator-publishedClass IIIRecallStatus · active
- Issuing authority
- Egyptian Drug Authority (EDA)
- Authority reference
- Periodic report no.(33) For 2026
- Date issued
- Apr 2026
- Recorded by us
- 2026-09-06 19:45:29 UTC
- Product
- Infusion pump set with Regulator
- 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
- Not published with the notice
- Expiry dates
- Not published with the notice
- Action type
- Recall
- Classification
- Class III as issued
- 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
- Egypt — no market beyond the issuing country was named on the notice
- Cross-border event
- Not linked to a cross-border event
- Notice text
- Infusion pump set with Regulator
0325و0925
كيو للصناعات البلاستيكية
R103433Lrc22V1
عدم مطابقة هذه التشغيلات لبيانات اخطار
التسجيل الخاصة بالمنتج و عدم مطابقتها
للماكيت المعتمد
وقف تداول و ضبط وتحريزالتشغيلة من
المستلزم الصادر لها عدم مطابقة
في حالة الشك في المستحضر الصيدلىيتم
الرجوع إلى هيئة الدواء المصرية سواء بالإتصال
بالخط الساخن 15301او الموقع الإلكترونى
الخاص بالهيئة.
أبريل 2026
اسم المستحضر
الشركة صاحبة المستلزم
سبب التحذير
الإجراءات
التصحيحية
نصائح
للمستهلكين
منشور
سحب
هذا التنبية خاص بالتشغيلات الواردة في المنشور فقط ولا ينطبق على
تداول المستحضر بشكل عام
رقم التسجيل المدون
على العبوات
ارقام LOT المدونة
على العبواتOriginal language: ar
- Notice text in English
- Notice. Infusion pump set with regulator, of Q for Plastic Industries, batches 0325 and 0925, reference R103433Lrc22V1. These batches do not conform to the particulars of the product's registration notification, nor to the approved artwork.Machine translation, produced by Drug Eye Africa and not checked by the issuing authority. The authority stated only the text above it.
- Status
- Active
- Superseded by
- Not superseded. This is the current version.
- Version
- 3
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
- c1093aa0e979ed3a213735f9e8acabf435395313ec9b7df9038a5dd7fefe1c14SHA-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 20:49:30 UTC
Cite this record
Drug Eye Africa (2026). DEA-EG-2026-0033: Infusion pump set with Regulator — Recall, Egyptian Drug Authority. Register of African Regulatory Actions. https://drugeyeafrica.org/register/notice/eg/2026/dea-eg-2026-0033Version 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.