Device recall

Z-1453-2015: Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign…

FDA device recall · Class II · US Endoscopy Group Inc

Key facts

Recall number (Z-number) Z-1453-2015
Recall event 70872
Product Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract.
Product code OCZ
Recalling firm US Endoscopy Group Inc
Recall class Class II
Status Terminated
Termination date Oct 27, 2016
510(k) numbers K962676
FEI number 1000122656

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 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)