Fresh Recalls

Olympus Ellik Evacuator Includes Glass Body: recall status

Notice names this product. Olympus of the Americas’s Olympus Ellik Evacuator Includes Glass Body is named in FDA Class II recall Z-2720-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices. Identifying details: Model Number: 194. UDI-DI: 0082192500586. All Lot Numbers.. Units affected: 3,241 units. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Olympus Ellik Evacuator Includes Glass Body
Company / brand
Olympus of the Americas
Lot / serial / date codes
Model Number: 194. UDI-DI: 0082192500586. All Lot Numbers.
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Japan, EU, and Latin America.
Agency product description and boundaries

Olympus Ellik Evacuator Includes Glass Body, Male Connecting Tubing & Latex Bulb. Model Number: 194.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
Olympus of the Americas

Recalls naming this model

FDA Class II · Medical device · July 22, 2026

Olympus Ellik Evacuator Includes Glass Body recall — Olympus Corporation of the Americas

Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.

Company / brand: Olympus of the Americas

Affected product: Olympus Ellik Evacuator Includes Glass Body

Official ID Z-2720-2026 · Official record ↗

See all Olympus of the Americas recalls →

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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.