Reported Jun 24, 2026 · Ongoing
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number:…
ConMed Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: ConMed Corporation · 525 French Rd · Utica, NY · 13502-5945
Is this the product you have?
- ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length
- Catalog NumberiAS5-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy
- Lot codes and dates
- Catalog NumberiAS5-120LP
- UDI-DI10845854045657
- Lot Numbers
159 of 159 codes
202504214202511075202510254202510274202510244202511104202601084202506054202506114202506104202505164202505294202505154202505176202507174202507184202507214202507044202506244202507024202507034202510024202510104202509194202507314202508134202508144202509224202509164202508294202509084202507315202507294202410094202410254202411114202409254202409255202505014202504224202502174202502254202504034202408234202501145202412124202408305202511064202510234202409114202409126202410174202510084202407105202502115202411194202508154202502134202502145202501174
- added 06/10/2026 expansion202407015, 202506104, 202501024, 202510244, 202511104, 202510274, 202508144, 202510024, 202510104, 202507034, 202507184, 202505054, 202505164, 202506244, 202412064, 202412184, 202408025, 202510254, 202507314, 202507044, 202503244, 202409256, 202509154, 202507315, 202506174, 202510074, 202412175, 202501305, 202504034, 202505154, 202407224, 202407105, 202505014, 202501316, 202502245, 202511065, 202409254, 202411194, 202410254, 202409114, 202511075, 202507214, 202407104, 202601084, 202412054, 202509164, 202504305, 202505294, 202408225, 202407024, 202509084, 202504304, 202502115, 202408054, 202509014, 202410255, 202601094, 202409125, 202408015, 202406245, 202510014, 202410245, 202501315, 202502016, 202410244, 202508284, 202409124, 202503245, 202502134, 202509224, 202502145, 202409136, 202412055, 202411085, 202508014, 202410094, 202507024, 202509194, 202508134, 202507174, 202501154, 202501304, 202501295, 202506114, 202504214, 202506054, 202505176, 202412165, 202409024, 202501025, 202412235, 202408235, 202410165, 202501145, 202406254. Manufactured from 14 June 2024 to 12 January 2026
- Amount recalled
- 32,792 packs (196,751 eaches)
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential for overpressure alerts.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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