Device recall

Z-0067-2017: The Introes Pocket Bougie is an endotracheal tube introducer. The device is an…

FDA device recall · Class II · Brathwaites Oliver Medical

Key facts

Recall number (Z-number) Z-0067-2017
Recall event 75148
Product The Introes Pocket Bougie is an endotracheal tube introducer. The device is an endotracheal tube introducer and it is used as a guide during intubation. Anesthesiology.
Product code BSR
Recalling firm Brathwaites Oliver Medical
Recall class Class II
Status Terminated
Termination date Jul 19, 2019
FEI number 3003213883

At a glance

  • None 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)