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Health product recall

LIAISON Estradiol II Gen (2016-07-13)

Starting date:
July 13, 2016
Posting date:
July 29, 2016
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-59610

Affected products

A. LIAISON Estradiol II Gen

Reason

The drug fulvestrant (Faslodex) has recently been shown to cross-react with estradiol leading to falsely elevated test results in estradiol assays.

Affected products

A. LIAISON Estradiol II Gen

Lot or serial number

Not Applicable

Model or catalog number

310680

Companies
Manufacturer

Diasorin Inc.

1951 Northwestern Avenue, P.O. Box 285

Stillwater

55082

Minnesota

UNITED STATES