FDAClass II · Medical device · Recall Z-2464-2026 · Recalled June 24, 2026

ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall — ConMed Corporation

Agency report date: June 24, 2026.

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: ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip
Company / brand: ConMed
Lot / serial / date codes: Catalog Number: iASB5-150. UDI-DI: 10845854045695. Lot Numbers: 202510144, 202508124, 202501144, 202408144, 202412044, 202505064, 202511284. *OUS added 06/10/2026 expansion: 202408144, 202501144, 202505064, 202508124, 202510144. Manufactured from 14 June 2024 to 12 January 2026.
Distribution: Nationwide distribution. International distribution to Australia, Austria, Belgium, Bosnia and Herzegovina, Canada, CHILE, CHINA, COLOMBIA, Croatia, Denmark, DOMINICAN REPUBLIC, ECUADOR, Egypt, Estonia, Finland, France, Germany, Greece, HONG KONG, India, INDONESIA, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Libya, Luxembourg, MALAYSIA, Malta, Montenegro, Netherlands, NEW ZEALAND, Norway, Oman, Palestine, PANAMA, PHILIPPINES, Poland, Qatar, Romania, Russia, Saudi Arabia, Serbia, SINGAPORE, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, TAIWAN,PROVINCE OF CHINA, THAILAND, Turkey, Ukraine, UNITED ARAB EMIRATES, United Kingdom. .

Agency product description and boundaries

ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy

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.

2. Agency hazard and consumer action

FDA reports: Potential for overpressure alerts.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2464-2026
Brand: All ConMed recalls
Classification: Class II
Units affected: 497 packs (2,982 eaches)
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall status

Companies & origin

Recalling firm location: Utica, NY, United States
Firm address: 525 French Rd, 13502-5945

Identifying details (verbatim from the notice)

Product codes / lots: Catalog Number: iASB5-150. UDI-DI: 10845854045695. Lot Numbers: 202510144, 202508124, 202501144, 202408144, 202412044, 202505064, 202511284. *OUS added 06/10/2026 expansion: 202408144, 202501144, 202505064, 202508124, 202510144. Manufactured from 14 June 2024 to 12 January 2026.
Distribution: Nationwide distribution. International distribution to Australia, Austria, Belgium, Bosnia and Herzegovina, Canada, CHILE, CHINA, COLOMBIA, Croatia, Denmark, DOMINICAN REPUBLIC, ECUADOR, Egypt, Estonia, Finland, France, Germany, Greece, HONG KONG, India, INDONESIA, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Libya, Luxembourg, MALAYSIA, Malta, Montenegro, Netherlands, NEW ZEALAND, Norway, Oman, Palestine, PANAMA, PHILIPPINES, Poland, Qatar, Romania, Russia, Saudi Arabia, Serbia, SINGAPORE, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, TAIWAN,PROVINCE OF CHINA, THAILAND, Turkey, Ukraine, UNITED ARAB EMIRATES, United Kingdom. .
Firm notified the public via: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID: 98854
Recall initiated: May 14, 2026
FDA classified: June 17, 2026
FDA report date: June 24, 2026

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Description/REF recall — ARROW INTERNATIONAL, LLCFDA · June 24, 2026
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Verify with the official sources:

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FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 22, 2026 at 6:00 PM UTC.

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