Data Foundry

Medical device recalls 2024

ESG-410 Electrosurgical Generator- In conjunction with… — Class II medical device recall Z-2415-2024

Ongoing recall by Olympus Corporation of the Americas, reported 2024-07-31, distributed nationwide. Electrosurgical Generators ESG-410 does not power on upon use, may result in delays in initiating treatment or

Recall numberZ-2415-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmOlympus Corporation of the Americas, Center Valley, PA, United States
Recall initiated2024-06-21
Classified2024-07-23
Reported by FDA2024-07-31
DistributedNationwide (US)
Quantity86
UPC / GTIN / UDI-DI04042761086349
Serial numbers102364, 102366, 102369, 102371, 102372, 102392, 102393, 102394, 102396, 102400, 102401, 102403, 102404, 102405, 102407, 102408, 102409, 102410, 102412, 102416, 102417, 102418, 102419, 102420, 102422 and 61 more
Model numbersWA91307C

Product

ESG-410 Electrosurgical Generator- In conjunction with electrosurgical accessories intended for cutting and coagulation of tissue in open, laparoscopic , and endoscopic surgeries Model/Catalog Number: WA91307C

Reason for recall

Electrosurgical Generators ESG-410 does not power on upon use, may result in delays in initiating treatment or prolonged surgery

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2415-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.