Device recall

Z-2465-2026: ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length…

FDA device recall · Class II · ConMed Corporation

Key facts

Recall number (Z-number) Z-2465-2026
Recall event 98854
Product ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Product code HIF
Recalling firm ConMed Corporation
Recall class Class II
Status Open, Classified
510(k) numbers K143404
FEI number 3001451571

At a glance

  • 1–9 Linked 510(k)s
  • 10–99 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)