Liaison Q.S.E.T. Device Plus
Brand(s)
Last updated
Summary
Product
Liaison Q.S.E.T. Device Plus
Issue
Medical devices - Labelling and packaging
What to do
Instructions provided by manufacturer on inspecting and disposing of any affected devices.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Liaison Q.S.E.T. Device Plus | 229224 225084 217134 224124 221294 230094 210204 223274 224244 232094 234114 221214 236174 259144 228174 | 319060 |
Issue
An investigation determined that 0.14% of the Liaison® Q.S.E.T. device plus in the lots identified have loose clear caps. The loose clear caps may allow leakage of the buffer from the tube.
Recall start date: November 7, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Chemistry
Companies
| Diasorin Inc. |
| 1951 Northwestern Avenue, Stillwater, Minnesota, United States, 55082 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76640
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