OXOID™ Agglutinating Sera, Salmonella 9-0

OXOID™ Agglutinating Sera, Salmonella 9-0

Company name & Address: registration number Batch number(s) Expiry date Pack size First release date Re-call Classification Recall date
Bioweb (Pty) Ltd

Ridgeview Office Park

248 Kent Avenue

Unit 10

Randburg

2194

 

N/A

 

6253410

 

02 June 2028

 

2ml

 

Not available

 

Class III Type C

 

04 May 2026

 

Brief description of the problem (reason for recall)

This recall has been initiated following an internal technical investigation, which determined that product R30957301 OXOID™ Agglutinating Sera Salmonella 9-0 does not meet IFU performance criteria, as it shows cross-reactions with 2-0 within 60 seconds.

Advice for health professionals and distributors:

Bioweb requests that you refrain from selling any of the affected batch(s) of OxoidTM Agglutinating Sera, Salmonella 9-0 and return them to your supplying warehouse or distributor with immediate effect. Bioweb (Pty) Ltd will collect all your stock which will be replaced with immediate effect.

For further product information, please call Bioweb on 0824107061.

 

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: 04/05/2026
File Type: www
Category: Product Recall
Unit: General ECTD & human medicines, Regulatory Compliance