Monofer 500mg/5ml (Iron (III) isomaltoside)

Monofer 500mg/5ml (Iron (III) isomaltoside)

 

Company name & Address:

 

Registration number

 

Batch number(s)

 

Expiry date

 

Pack size

 

First distributed

 

Re-call Classification

 

Recall date

 

Date Published

Acino Pharma (Pty) Ltd, No 106, 16th Road, Midrand, 1686, Gauteng, South Africa 46/8.3/0167 230504A-5  

May 2026

 

 

5ml (5 vials per carton)  

16 May 2024

 

 

Class III Type B 16 September 2024 14 October 2024

 

Reason for recalls

This recall is initiated as a result of a customer complaint reported within Poland. The customer complaint relates to a glass piece found in one (1) vial.

 

Advice to HCPs/Distributors/Public

You are requested to take the following action with regards to the affected batch:

  • Return the affected product to your supplying distributor/wholesaler for a credit.
  • If any of the recalled stock could have been transferred from your hospital to another, please inform them of this recall alternatively inform Acino and provide us with their details

 

Proposed action taken and its urgency: A SAHPRA approved recall letter was distributed to all distribution points and the recall process was initiated.

 

Reporting side effects

Public and healthcare professionals are encouraged to report any side effects after using a health product or after immunisation by using the Med Safety App. Your report will contribute to our monitoring of these health products.

Download latest version
Version: 1
Date Updated: 14/10/2024
File Type: www
Category: Product Recall
Unit: General ECTD & human medicines, Regulatory Compliance