FDA recall record

Kirwan Surgical Products Walcott Bipolar Pencil 25 Gauge Straight recall — FDA Z-0658-2025

Potential for the outer stainless-steel tube to break or detach.

Class Iclassification
Z-0658-2025official record ID
Dec 25, 2024report date

Recall record at a glance

Official recordZ-0658-2025
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmKirwan Surgical Products, LLC
Report dateDec 25, 2024
Recall initiation dateNov 14, 2024
Quantity3,010 units
LocationMarshfield, MA, United States

Official product description

Walcott Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: RX14-5011. Product Description: The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauterization of the retinal area during surgical procedures. The current line of pencils all have the same molded handle. The pencils' tip outer diameter is 25 gauge.

Why the product was recalled

Potential for the outer stainless-steel tube to break or detach.

Distribution information

Worldwide - US Nationwide including PUERTO RICO; AUSTRALIA, CANADA, CHILE, COLOMBIA, DENMARK, EGYPT, ENGLAND, FRANCE, GERMANY, ISRAEL, ITALY, JAPAN, MEXICO, NETHERLANDS, PHILIPPINES, SOUTH AFRICA, SWITZERLAND, TAIWAN, THAILAND, TRINIDAD, TURKEY, UNITED ARAB EMIRATES, and VENEZUELA.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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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