FDA recall record

Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Laser Products recall — FDA Z-1698-2016

Failure to provide the required instructions specifying a procedure and schedule for calibration of the measurement system.

Class IIclassification
Z-1698-2016official record ID
Jun 15, 2016report date

Recall record at a glance

Official recordZ-1698-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEllipse A/S
Report dateJun 15, 2016
Recall initiation dateMay 5, 2016
QuantityUS - 25
LocationHorsholm, N/A, Denmark

Official product description

Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Laser Products.

Why the product was recalled

Failure to provide the required instructions specifying a procedure and schedule for calibration of the measurement system.

Distribution information

Nationwide Distribution to the states of : NJ, PA, MI, CO, CA, FL, OK, NY, NH, CT, AZ and MO.

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

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

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