FDA recall record

Angiodynamics VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog No.: EVLT55OPS recall — FDA Z-1819-2022

OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not meet the required dimensional specification, may result in damage to the sheath,…

Class IIclassification
Z-1819-2022official record ID
Oct 5, 2022report date

Recall record at a glance

Official recordZ-1819-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAngiodynamics, Inc.
Report dateOct 5, 2022
Recall initiation dateAug 10, 2022
Quantity40 units
LocationQueensbury, NY, United States

Official product description

VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog No.: EVLT55OPS (each box contains 5 Procedure Kits). For use in the treatment of varicose veins.

Why the product was recalled

OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not meet the required dimensional specification, may result in damage to the sheath, including separation or the inability to move the fiber within the sheath. A damaged sheath will necessitate removal from the patient, which may result in procedural delay and/or surgical intervention

Distribution information

US Nationwide distribution in the states of FL, NC, NJ, NM, NY, PA, TX, VA.

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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