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Recall of automated peritoneal dialysis system
11
August 2010
The Department of Health (DH) received a notification from Baxter
Healthcare Limited (Hong Kong) (Baxter) this afternoon (August 11)
that it would organise with customers the return and replacement
of an automated peritoneal dialysis system, HomeChoice (product
code: 5C4474).
Baxter explained that the arrangement was necessary because the
required final tests and calibration of the product model had not
been performed, a spokesman for the department said.
Through network searching, the DH also noticed that the US Food
and Drug Administration (FDA) had actually issued an alert earlier
on this year concerning reports of serious injuries and at least
one death linked to increased intraperitoneal volume (IIPV) associated
with the use of the same model.
IIPV can cause serious breathing and heart problems which can result
in serious injury or death.
In addition, children and nonverbal patients may be at increased
risk because of their smaller abdominal cavities or inability to
communicate.
According to Baxter, at least 186 HomeChoice devices had been affected
in Hong Kong.
So far, the DH and Baxter have not received any report of adverse
events related to this issue.
Taking into account the information available, DH is concerned
with possible safety, efficacy and quality of the product, he said.
While seeking further clarification from FDA and the Baxter of
two events, DH in fact instructed Baxter to recall and replace the
device concerned.
"Patients using the device are urged to contact their attending
doctors immediately," the spokesman said.
"As an interim, clinicians are advised to balance the risks
and benefits to continued use of these devices by their patients
versus other forms of dialysis therapy.
"They should also review the prescription settings for patients
who continue to use these devices," he said.
Baxter's local supplier has set up a hotline, 6113 1063, for public
enquires.
The DH will closely monitor the progress of the recall.
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