FDA recall record

Alere Triage Total 5 Control Level 1, Model No. 88753 Description of the product: The Triage recall — FDA Z-0588-2017

Encoded with incorrect ranges that are not consistent with the ranges printed on the Expected Value Card.

Class IIclassification
Z-0588-2017official record ID
Nov 23, 2016report date

Recall record at a glance

Official recordZ-0588-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAlere San Diego, Inc.
Report dateNov 23, 2016
Recall initiation dateOct 12, 2016
Quantity513 kits
LocationSan Diego, CA, United States

Official product description

Alere Triage Total 5 Control Level 1, Model No. 88753 Description of the product: The Triage Total Controls 5 are quality control materials that are used to assist the laboratory in monitoring test performance throughout the measurable range. They are not calibrators and are not used to calibrate the Triage tests. The results of quality control testing do not impact direct patient care and should not influence clinical decision making process the physician uses to make clinical diagnosis for the patient. Indications for Use: The Alere Triage Total 5 Controls are assayed materials to be used with the Alere Triage Cardiac Panel, Alere Triage CardioProfiler Panel, Alere Triage Profiler SOB Panel, Alere Triage BNP Test, Alere Triage D-Dimer Test, and Alere Triage Meters to assist the laboratory in monitoring test performance.

Why the product was recalled

Encoded with incorrect ranges that are not consistent with the ranges printed on the Expected Value Card.

Distribution information

US Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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