ConMed Corporation: Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 230 VOLTS AC, REF/Catalog Number 7-900-230, Rx Only. There is no problem with the Hyfrecator 2000 Electrosurgical Units. -- ASSEMBLED IN MEXICO -- CONMED CORPORATION 525 FRENCH ROAD UTICA, NY 13502

Recall number

Z-1759-2017

Recalling firm

ConMed Corporation

Product

Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 230 VOLTS AC, REF/Catalog Number 7-900-230, Rx Only. There is no problem with the Hyfrecator 2000 Electrosurgical Units. -- ASSEMBLED IN MEXICO -- CONMED CORPORATION 525 FRENCH ROAD UTICA, NY 13502

Status

Terminated

Initiated

2017-02-28

Posted

not on file

Terminated

not on file

Reason

For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons were packaged in error by the manufacturer with non-sterile P/N 7-796-19 Handpiece Sheaths in pouches that were labeled as Sterile. This could cause an end user to use a non-sterile sheath as if it were sterile.

Root cause

Mixed-up of materials/components

Action

ConMed sent an URGENT: MEDICAL DEVICE RECALL Notices (dated 2/28/2017)to all affected US customers by USPS First Class Mail. International letters are in the process of translation and are scheduled to be sent by March 15, 2017. Customers were instructed to review their inventory for any of the affected product and were asked to complete the business reply form and return it to ConMed Corporation, 525 French Road, Utica, New York 13502. Customers with questions or requests should contact the Field Action Support Team at 1-800-448-6506, fax to 315-624-3225, or email hyfr2000@conmed.com. For questions regarding this recall call 315-624-3533.

Quantity

not on file

Distribution

Worldwide Distribution - US (nationwide) Internationally to Australia, Canada, Germany, Italy, UK, Great Britain, and Ireland.

Lot, serial or model codes

Serial Numbers: 1640179, 15500473, 16090084, 16140185, 16170283, 16250376, 16370476, 16380489, 1640180, 15510474, 16090085, 16140186, 16170284, 16250377, 16370477, 16380490, 1640181, 15510475, 16090086, 16140187, 16170285, 16250378, 16370478, 16380491, 1640182, 15510476, 16090087, 16140188, 16170286, 16260379, 16380479, 16380492, 1640183, 15510477, 16090088, 16140189, 16170287, 16260380, 16380480, 16480592, 1640184, 15510478, 16090089, 16140190, 16170288, 16260381, 16380481, 16480593, 1640185, 15510479, 16090090, 16140191, 16170289, 16260382, 16380482, 16480594, 1640186, 15510480, 16090091, 16140192, 16170290, 16260383, 16380483, 16480595, 1640187, 15510481, 16090092, 16140193, 16170291, 16260384, 16380484, 16480596, 1640188, 15510482, 16090093, 16140194, 16170292, 16260385, 16380485, 16480597, 15260015, 15510483, 16090094, 16140195, 16170293, 16260386, 16380486, 16480598, 15260016, 15510484, 16090095, 16140196, 16170294, 16260387, 16380487, 16480599, 15260018, 15510485, 16090096, 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16500612, 15280056, 16010005, 16090109, 16150210, 16190308, 16260401, 16430506, 16500613, 15280060, 16010006, 16090110, 16150211, 16190309, 16260402, 16430507, 16500614, 15280061, 16010007, 16090111, 16150212, 16190310, 16260403, 16430508, 16500615, 15280062, 16010008, 16090112, 16150213, 16190311, 16260404, 16430509, 16500616, 15280063, 16010009, 16090113, 16150214, 16190312, 16260405, 16430510, 16500617, 15330199, 16010010, 16090114, 16150215, 16190313, 16260406, 16430511, 16500618, 15330200, 16010011, 16090115, 16150216, 16190314, 16260407, 16430512, 16500619, 15330201, 16010012, 16090116, 16150217, 16190315, 16260408, 16430513, 16500637, 15330202, 16010013, 16090117, 16150218, 16190316, 16350409, 16440524, 16510620, 15330203, 16020014, 16090118, 16150219, 16190317, 16350410, 16440525, 16510621, 15340206, 16020015, 16090119, 16150220, 16190318, 16350411, 16440526, 16510622, 15340207, 16020016, 16090120, 16150221, 16210319, 16350412, 16440527, 16510623, 15340208, 16020017, 16090121, 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16160246, 16230328, 16360438, 16460554, 16510657, 15480437, 16050042, 16110147, 16160247, 16230339, 16360439, 16460555, 16510658, 15480438, 16050043, 16110148, 16160247, 16230340, 16360440, 16460556, 16510659, 15480438, 16050044, 16110149, 16160248, 16230341, 16360441, 16460557, 16510662, 15480439, 16050045, 16110150, 16160249, 16230342, 16360442, 16460558, 16510664, 15480440, 16050046, 16110151, 16160250, 16230343, 16360443, 16460559, 16510665, 15480441, 16050047, 16110152, 16160251, 16230344, 16360444, 16460560, 16520672, 15480442, 16050048, 16110153, 16160252, 16230345, 16360445, 16460561, 16520691, 15480443, 16050049, 16110154, 16160253, 16230346, 16360446, 16460562, 15500444, 16050050, 16110155, 16160254, 16230347, 16360447, 16460563, 15500445, 16050051, 16110156, 16160255, 16230348, 16360448, 16460564, 15500446, 16050052, 16110157, 16160256, 16230349, 16360449, 16460565, 15500447, 16050053, 16110158, 16160257, 16230350, 16360450, 16460566, 15500448, 16050054, 16140159, 16160258, 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510(k) numbers

["K963088"]

PMA numbers

not on file

Product code

GEI

Firm FEI

3001451571

Firm city

Utica

Firm state

NY

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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