FDA recall record

Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml recall — FDA Z-2487-2015

A reduction in the reconstituted stability has been identified. Clinicians may notice a drop in recovery of the control after reconstitution, which could…

Class IIclassification
Z-2487-2015official record ID
Sep 9, 2015report date

Recall record at a glance

Official recordZ-2487-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPointe Scientific, Inc.
Report dateSep 9, 2015
Recall initiation dateMay 19, 2015
Quantity2772 total vials (374 kits of 6 vials, 528 invidually sold vials)
LocationCanton, MI, United States

Official product description

Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml (2 vials each of Level 1, Level 2 and Level 3). Also sold as individual vials Bottle: Clear glass vials Cap: Rubber seal with colored aluminum seals Glucose-6-phosphate dehydrogenase (G6PD) controls can be used to test for the quantitative and qualitative determination of G6PD in blood.

Why the product was recalled

A reduction in the reconstituted stability has been identified. Clinicians may notice a drop in recovery of the control after reconstitution, which could result in an out of specification result prior to the current reconstitution claim of 7 days. For this reason we suggest discontinuing use of the control set.

Distribution information

Worldwide distribution: US (nationwide) including states of: PA, CA, KY, FL, NJ, DE, MI, MN,and IL; and countries of: United Arab Emirates, Austria, Italy, Israel, Greece, and Australia.

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

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