FDA recall record

Intuitive Surgical Tip Cover for 8mm Monopolar Curved Scissors (Hot Shears)Accessory recall — FDA Z-2339-2012

There is potential for the sterility of the product to be compromised.

Class IIclassification
Z-2339-2012official record ID
Sep 19, 2012report date

Recall record at a glance

Official recordZ-2339-2012
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIntuitive Surgical, Inc.
Report dateSep 19, 2012
Recall initiation dateAug 9, 2012
Quantity11,121 Boxes
LocationSunnyvale, CA, United States

Official product description

Tip Cover for 8mm Monopolar Curved Scissors (Hot Shears)Accessory, Disposable, 8mm MCS, Box of 10. The intended use of the Tip Cover Accessory is to provide dielectric insulation over a section of the Monopolar Curved Scissor instrument so that RF energy is only available at the scissor blades. The Monopolar Curved Scissors are intended for endoscopic manipulation of tissue, including: cutting, blunt and sharp dissection, electrocautery. This accessory is to be used with the Intuitive Surgical Endoscopic Instrument Control Systems (da Vinci, da Vinci S and da Vinci Si Surgical Systems Models IS1200, 12000, ISSOQO).

Why the product was recalled

There is potential for the sterility of the product to be compromised.

Distribution information

Worldwide Distribution-USA (nationwide) including Puerto Rico and the countries of Australia, Canada, and Lebanon

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: E-Mail.

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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