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FIAB SPA · Model F7234/1 · UDI-DI 18033695727449

GEI Prescription
1
510(k) clearances
119,015
Adverse events (469 deaths)
644
Recalls
862
Facilities

Description

HTC (high temperature cautery) F7234/1 model is a sterile bipolar battery operated disposable device for the cauterization of small vessels. The fine tip length 75mm permits the accurate and effective cauterization of very small vessels. Tip reaches a maximum working temperature of 1.200°C (2.200 °F). The cautery is suitable to be used all the times a quick and precise cauterization is necessary even in difficult access sites.

Recalls

DateFirmReason
2026-08-18Olympus Corporation of the AmericasPotential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.
2026-06-08Stryker CorporationThere has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
2026-06-08Stryker CorporationThere has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
2026-06-02Maquet Cardiovascular, LLCGetinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-2878
2026-03-23Olympus Corporation of the AmericasPotential for detachment of a distal tip component of the device during use.
2026-03-23Olympus Corporation of the AmericasPotential for detachment of a distal tip component of the device during use.
2026-03-23Olympus Corporation of the AmericasPotential for detachment of a distal tip component of the device during use.
2026-03-23Olympus Corporation of the AmericasPotential for detachment of a distal tip component of the device during use.
2026-02-25Olympus Corporation of the AmericasOlympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting For
2026-02-25Olympus Corporation of the AmericasOlympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting For

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.