FDA DevicesClass II

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Publicado: 24 de junio de 2026ID de Retiro: Z-2474-2026Categoría: Dispositivos MédicosPaís: Estados Unidos
US
Medical DeviceFDA DevicesUSUS

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Recalling Firm: ConMed Corporation

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Motivo del Retiro / Peligro

Potential for overpressure alerts.

Descripción del Producto e Identificación

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Additional Source Details

FieldValue
CityUtica
StateNY
Event id98854
Address 1525 French Rd
Code infoCatalog Number: iAS12-100LPI. UDI-DI: 10845854045640. Lot Numbers: 2025082210, 202502265, 202601074, 202512034, 202601084, 202512194, 202512184, 202512204, 202512224, 202512024, 2026010610, 2025100710, 202512094, 202512174, 2025121810, 202510214, 2026010511, 202510024, 202510104, 202510224, 202510084, 2025121710, 202510064, 202512104, 202512164, 202512064, 202512084, 202512054, 202512044, 202512154, 202510014, 202511144, 202511254, 202511264, 202510074, 202510144, 202511124, 202509094, 202509194, 202509294, 2025093010, 202509304, 202511134, 202511194, 202509084, 2025102310, 202510294, 202510304, 202510314, 202511046, 202511114, 2025101510, 202511154, 202511184, 202509184, 202510284, 202509174, 202511014, 202511044, 202511054, 202509044, 202509164, 202510274, 2025082210, 2025101310, 202509224, 2025092910, 202510134, 2025100610, 202508194, 202508234, 202509054, 202508184, 2025082110, 202508224, 202508144, 2025082010, 2025081110, 202508114, 202508134, 202508154, 202508054, 202508074, 2025... [TRUNCATED]
Postal code13502-5945
Report date20260624
Product typeDevices
Product quantity147,013 packs (882,078 eaches)
Reason for recallPotential for overpressure alerts.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260514
Initial firm notificationTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date20260617

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS...?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Devices). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Resumen

  • Empresa ResponsableConMed Corporation
  • StatusOngoing
  • Nivel de RiesgoClass II
  • DistributionNationwide 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. .
Recall Hazard Severity
High Alert (Class I)
Alerta Oficial de la Agencia

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🚨 SAFETY ALERT: ConMed Corporation - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

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https://therecallfile.com/es/recalls/conmed-airseal-12mm-access-port-and-palm-grip-obturator-with-bladeless/FDA-Z-2474-2026
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