FLOMIST NASAL SPRAY (Fluticasone Propionate 50 mcg/ spray)

FLOMIST NASAL SPRAY (Fluticasone Propionate 50 mcg/ spray)

                                 Company name & Address                           registration number                   Batch number                         Expiry date                                                           Pack size                                                                First distributed  

Re-call Classification

 

Recall date

 

Cipla Medpro (Pty) Ltd,  Parc du Cap Building 9, Mispel Street, Bellville, 7530, South Africa

 

37/21.5.1/0289

                       IC20685  

Nov.2024

 

1 x 120 MD

 

28 Sept.2022

 

Class II Type B

 

 

12.Dec. 2022

 

Reason for recall

The recall is due to an out of specification (OOS) result that was observed in Flomist nasal spray, batch no. IC20685. OOS result was observed in microbial enumeration test. The organism was identified as Burkholderia Cepacia

Cipla Medpro (Pty) Ltd, in South Africa took the decision to initiate a voluntary recall on batch IC20685.

 

Advice to HCPs/Distributors/Public:

The company requested their clients to refrain from selling or dispensing FLOMIST NASAL SPRAY, Batch No. IC20685 and to return all remaining stock to their supplying warehouse or distributor with immediate effect

 

Proposed action taken and its urgency: A SAHPRA approved recall letter distributed to all distribution points and recall 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: 12/12/2022
File Type: www
Category: Product Recall
Unit: General ECTD & human medicines, Regulatory Compliance