Public recall detail

Liaison Q.S.E.T. Device Plus

2024-12-04

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Recall Safety notice
Quick summary

Quick summary: Liaison Q.S.E.T. Device Plus. Date: 2024-12-04.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Liaison Q.S.E.T. Device Plus. Date: 2024-12-04.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandDiasorin Inc.
ProductLiaison Q.S.E.T. Device Plus
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-76640

Affected products

ProductLiaison Q.S.E.T. Device Plus
Lot229224 225084 217134 224124 221294 230094 210204 223274 224244 232094 234114 221214 236174 259144 228174
Model319060
Serial number229224 225084 217134 224124 221294 230094 210204 223274 224244 232094 234114 221214 236174 259144 228174
DescriptionLiaison Q.S.E.T. Device Plus

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

What you should do

  • Instructions provided by manufacturer on inspecting and disposing of any affected devices.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Chemistry
CompaniesDiasorin Inc. 1951 Northwestern Avenue, Stillwater, Minnesota, United States, 55082
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-76640
Background{}
CompaniesDiasorin Inc. 1951 Northwestern Avenue, Stillwater, Minnesota, United States, 55082
AudiencesHealthcare
Source updated2024-12-04

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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