FDA recall record

The Binding Site Group Human Alpha-1-Antitrypsin Kit for use on the SPAPlus analyser recall — FDA Z-0002-2018

The high control for the kit is recovering low and may be out of range for assigned values.

Class IIclassification
Z-0002-2018official record ID
Oct 11, 2017report date

Recall record at a glance

Official recordZ-0002-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThe Binding Site Group, Ltd.
Report dateOct 11, 2017
Recall initiation dateAug 23, 2017
Quantity361 kits
LocationBirmingham, N/A, United Kingdom

Official product description

Human Alpha-1-Antitrypsin Kit for use on the SPAPlus analyser, Product #NK034.S. The firm name on the label is The Binding Site Group Ltd., Birmingham, UK. Product is designed for the quantitative in-vitro determination of Alpha-1-antitrypsin in human serum using the SPAPLUS turbidimetric analyser. The measurement of Alpha-1-antitrypsin aids in the diagnosis of several conditions including adult cirrhosis of the liver. In addition, Alpha-1-antitrypsin deficiency has been associated with pulmonary emphysema. This test should be used in conjunction with other laboratory and clinical findings.

Why the product was recalled

The high control for the kit is recovering low and may be out of range for assigned values.

Distribution information

Worldwide Distribution - US Distribution to the state of CA., and to the countries of : United Kingdom, Germany, France, Czech Republic, Belgium, Panama, Bulgaria, Iran, Argentina, Turkey Romania, Colombia, and Saudi Arabia.

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: E-Mail.

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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