FDA recall record

Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analytical X-Ray recall — FDA Z-0680-2017

Possible unintentional x-ray emission after users attempt early termination of the sequence.

Class IIclassification
Z-0680-2017official record ID
Dec 14, 2016report date

Recall record at a glance

Official recordZ-0680-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmOlympus Scientific Solutions Americas
Report dateDec 14, 2016
Recall initiation dateOct 27, 2016
Quantity41 units
LocationWaltham, MA, United States

Official product description

Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analytical X-Ray System

Why the product was recalled

Possible unintentional x-ray emission after users attempt early termination of the sequence.

Distribution information

US Distribution to the states of : TX, WA, GA, MA, SC, AZ, PA, VA, CA, OH, NJ, MD, CO, IL, LA, and MN.

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: FDA Mandated. Initial notification: Letter.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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