Device recall

Z-0414-2007: AutoSuture Bladed Trocar, equipped with safety shield. Model number 179094…

FDA device recall · Class II · Ascent Healthcare Solutions, Inc.

Key facts

Recall number (Z-number) Z-0414-2007
Recall event 37162
Product AutoSuture Bladed Trocar, equipped with safety shield. Model number 179094. Available with smooth or threaded sleeve in sizes 5-15mm inner diameter and 70-100mm length.
Product code NLM
Recalling firm Ascent Healthcare Solutions, Inc.
Recall class Class II
Status Terminated
Termination date Oct 31, 2008
510(k) numbers K043594
FEI number 1000132435

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

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