Data Foundry

Medical device recalls 2026

ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip — Class II medical device recall Z-2464-2026

Ongoing recall by ConMed Corporation, reported 2026-06-24, distributed nationwide. Potential for overpressure alerts.

Recall numberZ-2464-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmConMed Corporation, Utica, NY, United States
Recall initiated2026-05-14
Classified2026-06-17
Reported by FDA2026-06-24
DistributedNationwide (US)
Countries outside the USAE, AT, AU, BE, CA, CH, CL, CN, CO, DE, DK, DO, EC, EE, EG, ES, FI, FR, GB, GR, HK, HR, ID, IE, IL, IN, IQ, IT, JO, JP, KR, KW, LB, LU, MT, MY, NL, NO, NZ, OM, PA, PH, PL, QA, RO, RS, RU, SA, SE, SG, SK, TH, TR, TW, UA, ZA
UPC / GTIN / UDI-DI10845854045695
Lot numbers202408144, 202412044, 202501144, 202505064, 202508124, 202510144, 202511284
Model numbersIASB5-150

Product

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

Reason for recall

Potential for overpressure alerts.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2464-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.