Recall some batches of LINZESS products

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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,

  1. Consult your healthcare provider prior to discontinuing use of the affected batches, or for any health concerns.
  2. Contact the recalling firm or SFDA if you have any questions about the recall.
  3. 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).
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