Home/Recalls/FDA-Z-1442-2026
FDA DevicesClass II

Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. ...

Published: March 4, 2026Recall ID: Z-1442-2026Category: devicesCountry: US

Reason for Recall / Hazard

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

Product Description & Identification

Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applications.

Additional Source Details

FieldValue
CityCenter Valley
StatePA
Event id98288
Address 13500 Corporate Pkwy
Address 2N/A
Code infoModel No. A22041T; UDI: 04042761020978; All Lots.
Postal code18034-8229
Report date20260304
Product typeDevices
Product quantity2,626 units
Reason for recallComplaints of the ceramic tip of the resection sheath breaking have been received.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251111
Initial firm notificationLetter
Center classification date20260220

Overview

  • Recalling FirmOlympus Corporation of the Americas
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide Distribution.
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