FDA recall record

Olympus Scientific Solutions Americas Analytical X-ray System recall — FDA Z-1991-2015

Higher than published scatter around the probe head when testing some samples. At the point the customer would interact directly with the instrument…

Class IIclassification
Z-1991-2015official record ID
Aug 12, 2015report date

Recall record at a glance

Official recordZ-1991-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOlympus Scientific Solutions Americas
Report dateAug 12, 2015
Recall initiation dateJun 9, 2015
Quantity1047
LocationWaltham, MA, United States

Official product description

Olympus Scientific Solutions Americas Analytical X-ray System. Delta, Delta Element, Delta Plus, DPO-4000-XX-U-EN-EN-PM-SP12, DPO-6000-XX-U-EN-EN-AP-SP10. Mobile X-ray System.

Why the product was recalled

Higher than published scatter around the probe head when testing some samples. At the point the customer would interact directly with the instrument (Trigger position), most readings were lower. However, measurements around the probe head were higher particularly on samples know to be highly scattering (plastics, soils) with minimal increases on high density samples (steel, aluminum).

Distribution information

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

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About this record

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