Olympus M3 Gold Autoclavable Foroblique Telescope 30: Sterilization Parameter Discrepancy
Olympus recalls 72 units of M3 Gold Autoclavable Foroblique Telescope 30 (Model M3-30A) due to sterilization parameter discrepancies between instructions and Japanese package inserts.
Recall notice
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.
What happened, in plain English
Olympus is recalling 72 units of the M3 Gold Autoclavable Foroblique Telescope 30 (Model M3-30A) because sterilization parameters listed in the product instructions differ from those in the Japanese package insert. This discrepancy could lead to improper sterilization if the device is used in medical settings. Read more at govinfonow.com/recall/1449255-olympus-corporation-of-the-americas-recalls-olympus-m3-gold-autoclavable.
Source Summary by GovInfoNow · govinfonow.com/recall/1449255-olympus-corporation-of-the-americas-recalls-olympus-m3-gold-autoclavable · Updated October 14, 2026 · FDA enforcement record: FDA #Z-3299-2026
Cite this page
“Olympus M3 Gold Autoclavable Foroblique Telescope 30: Sterilization Parameter Discrepancy.” GovInfoNow, updated October 14, 2026. https://govinfonow.com/recall/1449255-olympus-corporation-of-the-americas-recalls-olympus-m3-gold-autoclavable. Based on FDA recall #Z-3299-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3299-2026%22&limit=1).
Why it’s dangerous
The sterilization parameters in the product instructions do not match those in the Japanese package insert. This mismatch could result in improper sterilization if the device is used in medical settings, potentially leading to contamination risks.
Who’s affected
Medical facilities using the Olympus M3 Gold Autoclavable Foroblique Telescope 30 (Model M3-30A) in Japan are likely affected. The risk is highest for healthcare providers who rely on this device for sterilization processes.
How to tell if you have this one
Check for the model number M3-30A on the device. The product was distributed internationally to Japan and includes all serial numbers.
- Brand
Olympus- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
International distribution to the country of Japan.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-3299-2026 | Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A.; Model Number: M3-30A. UDI-DI: 00821925005679. All Serial Numbers. | 72 units |
| Z-3300-2026 | Olympus M3 Gold Autoclavable Lateral Telescope 70. Model Number: M3-70A.; Model Number: M3-70A. UDI-DI: 00821925005686. All Serial Numbers. | 50 units |
What to do — step by step
Check Device Details
Verify the model number M3-30A on the device and confirm it was distributed to Japan.
How this recall unfolded
Recall timeline
FDA published this recall 44 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-3299-2026 (August 24, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3299-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.