Device recall

Z-0244-2007: Rusch (Latex Free) Neoprene Pecan Shaped Breathing Bag with 15 mm neck insert…

FDA device recall · Class II · Teleflex Medical

Key facts

Recall number (Z-number) Z-0244-2007
Recall event 36788
Product Rusch (Latex Free) Neoprene Pecan Shaped Breathing Bag with 15 mm neck insert, size 1 liter; a rebreathing bag; Teleflex Medical, Bannockburn, IL 60015 USA, Made in UK
Product code BYW
Recalling firm Teleflex Medical
Recall class Class II
Status Terminated
Termination date Nov 30, 2007
FEI number 3004959265

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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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