Homechoice Automated PD set with cassette and 4-Prong luers

Homechoice Automated PD set with cassette and 4-Prong luers

Company name & Address: registration number Batch number(s) Expiry date Pack size First release date Re-call Classification Recall date
Adcock Ingram Critical Care

1 Sabax Road

Aeroton

Johannesburg

2013

South Africa

 

N/A

 

25L02T005
25L06T017
26A02T005

 

25L02T005 (NOV 2030)
25L06T017 (NOV 2030)
26A02T005 (DEC 2030)

 

1’s

 

25L02T005(21 APR 2026)
25L06T017 (09 APR 2026)
26A02T005 (22 APR 2026)

 

Class III Type C

 

20 July 2026

 

Brief description of the problem (reason for recall)

Adcock Ingram Critical Care (AICC) is issuing a Medical Device Recall as the distributor for certain lots of HomeChoice Sets with 4-prong Cassettes due to an issue associated with an increase of reports of alarms while using the HomeChoice cycler. The most frequent alarms, “Check Lines & Bags” and “Reload the Set 156”, may occur and repeated alarms could prevent the HomeChoice system from initiating the therapy cycle.

 

Advice for health professionals and distributors:

The manufacturer, Vantive, has determined that this issue is caused only by specific cassettes from lots listed in the affected product table below: This issue could lead to a delay or interruption of therapy. In addition, it may potentially lead to touch contamination of the sterile fluid path due to failure of following aseptic technique as stipulated in the Patient Guide as a result of having to repeatedly change sets.

 

If any of the above batches have been received, please quarantine and isolate the impacted batch. Please contact the people below to arrange for upliftment and credit of the units.

 

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: 20/07/2026
File Type: pdf
Category: Product Recall
Unit: Medical Devices, Regulatory Compliance