—#154555

Product

Dimension Vista Digoxin (DIGXN) Flex reagent cartridge

FDA product code: KXT — Enzyme Immunoassay, Digoxin
Device class: Class 2
Medical specialty: Clinical Toxicology
510(k) numbers: K093441
Affected lot / code info: Device Listing Number # D098364 Lot # 16103BD, 16195BB, 16230BA, 16259BD, 16320BD, 16363BA

Why it was recalled

The concentrations for Biotin listed in the Non-Interfering Substances section of the current Dimension and Dimension Vistat Instructions for Use (IFU) for Dimension TNI, Dimension Vista DIGXN, E2, FERR, PRL, and TSH have incorrect units, and incorrectly state the level at which biotin does not interfere.

Root cause (FDA determination)

Under Investigation by firm

Action the firm took

Siemens mailed an Urgent Medical Device Correction Letter to affected customers on 03/29/2017 to inform them of the issue. The notice explained the reason for the field action, Risk to Health and actions to be taken by the customer.

Recalling firm

Firm: Siemens Healthcare Diagnostics, Inc.
Address: 500 Gbc Dr PO BOX 6101, Ms 514, Newark, Delaware 19702-2466

Distribution

Distribution pattern: Product was distributed throughout the United States and Canada, United Arab Emirates, Argentina, Austria,Australia,Bangladesh,Belgium,Brazil,Canada Switzerland,China,Columbia,Czech Republic,Germany,Denmark,Algeria Egypt,Spain,Finland,France,Great Britain,Greece,Croatia,Indonesia,Ireland India,Italy,Japan,Canary Islands,Republic of Korea,Kuwait,Lebanon,Latvia Macedonia,Netherlands,Norway,New Zealand,Philippines,Poland,Portugal Qatar,Saudi Arabia,Slovenia,Slovakia,Turkey,Taiwan,South Africa

Timeline

Recall initiated: 2017-03-21
Posted by FDA: 2017-05-05
Terminated: 2018-08-03
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #154555. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.