Safety Alert for Mona Lisa intrauterine contraceptive devices

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by CNWFE.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

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  • Type of Event
    Safety alert
  • Date
    2011-07-29
  • Event Country
  • Event Source
    DH
  • Event Source URL
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • Extra notes in the data
    Press release
  • Reason
    Recall of two mona lisa intrauterine contraceptive devices (with photo) the department of health (dh) today (july 29) instructed a local medical devices supplier, cnw far east limited (cnwfe), to recall all batches of two of its intrauterine contraceptive devices (iucds), mona lisa cut 380a and mona lisa nt cu 380, from shelves following discovery of mislabelling and wrong packaging involving the two models. the discovery was by the dh's chai wan maternal and child health centre (mchc) when they served a family planning client yesterday. on opening a cut 380a package, staff discovered that an nt cu 380 device was found instead. "cut 380a has a life span of 10 years while nt cu 380 has only half that - five years," a dh spokesman stated. "as the client had expressed no preference on her choice, the nt cu 380 was inserted and she was also told so." being unusual, the incident was reported by the mchc to the medical device control office in the dh. the latter began investigation immediately and findings so far reveal that the entire production chain for mona lisa iucds actually takes place in belgium.   the spokesman said that although the two devices differ only in terms of life span and the dh is not aware of related notifications here or worldwide, to be prudent, the client was contacted. she opted for an alternative mode of contraception on learning of the matter.   "moreover, we have referred the case to our belgian counterpart for their follow-up action. meanwhile, cnwfe is also instructed to recall both products from shelves, pending investigation findings in belgium. however, at present, there is no evidence to indicate that clients with the devices inserted require removal," the spokesman said. given that sales records show that the devices have been distributed to health-care institutions and private doctors, the dh has brought the matter to relevant stakeholders' attention. "health-care professionals and retailers should stop supplying the said products to clients immediately. cnwfe has set up a hotline, 2388 2933, to answer related enquiries," the spokesman said. "and to cater for enquiries from mchc's clients, the dh will also operate a hotline, 2125 1133, from tomorrow onward," the spokesman added. the spokesman emphasised that the dh will be monitoring the recall besides continuing the investigation with belgian collaboration. ends/friday, july 29, 2011 issued at hkt 21:37.

Device

  • Model / Serial
  • Product Description
    Press release: Recall of two Mona Lisa intrauterine contraceptive devices (with photo)
  • Manufacturer

Manufacturer