Class II recall Z-3299-2026: Olympus Corporation of the Americas

Class II recall Z-3299-2026: Olympus Corporation of the Americas (Pennsylvania): Olympus Corporation of the Americas. Dated 29 days ago, it is in the active follow-up window. Score 62/100. As of 2026-11-04, from U.S. FDA openFDA (510(k) clearances and device enforcement reports).

Data as of · Compiled by Zalwin from U.S. FDA openFDA (510(k) clearances and device enforcement reports)

Free preview: all 14 published fields of this record are shown below. Locked: 18 related PA FDAPulse records and the 5-column CSV export.

FieldValue
RecordDevice recall
Recall numberZ-3299-2026
Recalling firmOlympus Corporation of the Americas
ClassificationClass II
StatusOngoing
Voluntary / mandatedVoluntary: Firm initiated
SpecialtyOther
ProductOlympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A.
ReasonThere are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese package insert.
Quantity72 units
DistributionInternational distribution to the country of Japan.
Recall initiated2026-08-24
Reported2026-10-07
Firm locationCenter Valley, PA, United States
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  • Source agency: U.S. FDA openFDA (510(k) clearances and device enforcement reports)
  • Record date: 2026-10-07
  • Data refreshed: 2026-11-04
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) · Last refreshed: Wed, 04 Nov 2026 09:16:12 GMT

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Peer benchmark and outreach value: Class II recall Z-3299-2026: Olympus Corporation of the Americas and 19 Pennsylvania peers

  • Pennsylvania FDAPulse records like this one: 19
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every Pennsylvania peer: $3,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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62 / 100 Predicate Speed & CAPA Advisory Opportunity Score

  • Class II recall: usually triggers CAPA and quality-system remediation work.
  • Recall is still ongoing.
  • Posted 29 days ago.

What is the FDAPulse record for Class II recall Z-3299-2026: Olympus Corporation of the Americas in Pennsylvania?

Class II device recall Z-3299-2026 by Olympus Corporation of the Americas: There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the steri

How does Class II recall Z-3299-2026: Olympus Corporation of the Americas compare to other Pennsylvania FDAPulse records?

It is 29 days old, still within a typical 45-day follow-up window.

Class II recall Z-3299-2026 vs. top 3 peers

OrganizationLocationRecord date
Class II recall Z-3299-2026PA2026-10-07
Class II recall Z-3155-2026MA2026-10-07
Class II recall Z-0232-20272026-10-28
Class II recall Z-0243-20272026-10-28

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