Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U
Reported: November 6, 2024 Initiated: September 4, 2024 #Z-0264-2025
Product Description
Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U
Reason for Recall
There was an increase in complaints indicating an occurrence of system error E1226 "Could not write to Audio Buffer" during procedures using the ESG-410 (SEP).
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 279 units
- Distribution
- US Nationwide.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U. Recalled by Olympus Corporation of the Americas. Units affected: 279 units.
Why was this product recalled? ▼
There was an increase in complaints indicating an occurrence of system error E1226 "Could not write to Audio Buffer" during procedures using the ESG-410 (SEP).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 6, 2024. Severity: Moderate. Recall number: Z-0264-2025.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11