FDA Device recall Z-3300-2026
Olympus M3 Gold Autoclavable Lateral Telescope 70
- FDA Device
- Class II
- ongoing
- Published 2026-10-07
On 2026-10-07 the FDA classified a Class II recall of Olympus M3 Gold Autoclavable Lateral Telescope 70 by Olympus, citing there are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3300-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-08-24 |
| Published | 2026-10-07 |
| Last updated | 2026-10-13 05:30 UTC |
| Company | Olympus |
| Distribution | n/a |
Product
Olympus M3 Gold Autoclavable Lateral Telescope 70. Model Number: M3-70A.
Reason
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.
Identifiers
| code_info | Model Number: M3-70A. UDI-DI: 00821925005686. All Serial Numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-10-13 05:30 UTC. Current status: ongoing.
Other recalls by Olympus
- Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System
FDA Device · Class II · 2026-10-07 · Olympus - Olympus M3 Gold Autoclavable Foroblique Telescope 30
FDA Device · Class II · 2026-10-07 · Olympus - Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector
FDA Device · Class II · 2026-09-30 · Olympus - Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm
FDA Device · Class II · 2026-09-30 · Olympus - Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector
FDA Device · Class II · 2026-09-30 · Olympus
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3300-2026%22
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