Recall some batches of LINZESS products
2024-02-27Product Description :
الاسم التجاري |
الاسم العلمي |
رقم التسجيل |
رقم التشغيلة المتأثرة |
الشركة الصانعة |
Trade Name |
Scientific Name |
Register Number |
Affected batch number |
Manufacturer |
LINZESS 290 µg |
LINACLOTIDE |
Unregistered |
1173604 |
Forest Laboratories Ireland Limited |
A2022020 |
||||
LINZESS 145 µg |
1173004 |
|||
A2022016 |
Issue :
SFDA has issued a recall some batches of LINZESS products due to the affected batches are not comply with the required technical specifications. abbvie is voluntarily recalling the above batches.
Recommendations :
For healthcare professionals: Stop dispensing the affected batches immediately. Embargo/Quarantine all remaining stock. Affected batches should be returned to the supplier.
For patients,
- Consult your healthcare provider prior to discontinuing use of the affected batches, or for any health concerns.
- Contact the recalling firm or SFDA if you have any questions about the recall.
- Adverse reactions or quality problems experienced with the use of this product may be reported to Saudi Vigilance either online or call center (Call 19999).