Home / Recalls / Olympus Corporation of the Americas / Z-1439-2026

Z-1439-2026 Class II Ongoing

Recalled by Olympus Corporation of the Americas — Center Valley, PA

Recall Details

Product Type
Devices
Report Date
March 4, 2026
Initiation Date
November 11, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
6,949 units

Product Description

Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.

Reason for Recall

Complaints of the ceramic tip of the resection sheath breaking have been received.

Distribution Pattern

US Nationwide Distribution.

Code Information

Model No. A22040A; UDI: 04042761029339; All Lots.

Other recalls by Olympus Corporation of the Americas

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  • Z-1488-2026 Class II — Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box (January 29, 2026)
  • Z-1352-2026 Class I — Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflatio (January 16, 2026)
  • Z-1354-2026 Class I — Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflat (January 16, 2026)
  • Z-1353-2026 Class I — Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insuffla (January 16, 2026)
  • Z-1494-2026 Class II — Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Nam (January 8, 2026)
  • Z-1292-2026 Class II — Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411 (January 7, 2026)
  • Z-1270-2026 Class II — Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-4 (January 7, 2026)
  • Z-1288-2026 Class II — Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-4 (January 7, 2026)
  • Z-1271-2026 Class II — Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V41 (January 7, 2026)