FDA Enforcement Class II Terminated

Elecsys Vitamin D total II, Vitamin D Test System, Material number 07028148190 Product Usage: This assay is intended for the quantitative determination of total 25-hydroxyvitamin D in human serum and plasma. This assay is to be used as an aid in the assessment of vitamin D sufficiency in adults. The electrochemiluminescence binding assay is intended for use on the immunoassay analyzer.

Recall: Z-2389-2018 · Reported July 18, 2018

Enforcement

Recall Number
Z-2389-2018
Event ID
80008
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Roche Diagnostics Corporation
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 18, 2018
Initiation Date
April 27, 2018
Classification Date
July 8, 2018
Termination Date
May 11, 2020
Address
9115 Hague Rd, Indianapolis, IN, 46256-1025, United States

Description

Elecsys Vitamin D total II, Vitamin D Test System, Material number 07028148190 Product Usage: This assay is intended for the quantitative determination of total 25-hydroxyvitamin D in human serum and plasma. This assay is to be used as an aid in the assessment of vitamin D sufficiency in adults. The electrochemiluminescence binding assay is intended for use on the immunoassay analyzer.

Reason

The device may give a falsely elevated result that is non-reproducible. If vitamin D level is monitored by laboratory tests and adapted based on the result, a dosage reduction of vitamin D supplementation cannot be excluded, and as a consequence, vitamin D deficiency may develop over time.

Code Info

No specific lot codes. This issue affects users of the cobas e 801 module.

Distribution

US Nationwide distribution.

Quantity

347 units