28 Jul 2011
After assessing a notification from a local medical device supplier, Coloplast (Hong Kong) Ltd, about its proposal to recall one of its product Alterna R Sterile Post-Operative ostomy bag from consumers on sterility ground, the Department of Health (DH) endorses the action.
Coloplast, the manufacturer of the device under recall, found during routine product sterility test that a lot has failed. Investigation reveals that the failed lot of product was sterilised after January 2010, when the sterilisation process was moved over to a new site. Thus, Coloplast decides to conduct a recall of all products sterilised at the new site, though no report of any adverse incident arising from the use of ostomy bags produced in the new site has been received worldwide. DH also has not received any such notification locally.
The models under recall are 12808, 12810 and 12818, all with expiry date on 1 January 2013 or later.
Alterna R Sterile Post-Operative ostomy bag is used for collecting output from stoma - an opening created on the abdomen after bowel or urinary tract surgery in order to divert faeces or urine respectively.
A spokesman for DH said, "Since there is concern over the sterility of the product, with potential risk of infection, the Department endorses Coloplast (Hong Kong) Ltd’s recall as a measure to safeguard public health."
Coloplast (Hong Kong) Ltd's sales record shows that its products have been sold to both hospitals and patients here in Hong Kong.
"Customers who have the affected products in hand should return them to Coloplast (Hong Kong) Ltd. The company can be reached through its hotline at telephone number 3628-7436. People who have used the products
should also consult their healthcare professionals if feel unwell or in doubt," the spokesman advises.
DH has already alerted the Hospital Authority, private hospitals, relevant healthcare institutions and medical associations about the matter, and will closely monitor the recall besides continuing investigation.