Device recall

Z-2872-2017: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension…

FDA device recall · Class II · C.R. Bard, Inc.

Key facts

Recall number (Z-number) Z-2872-2017
Recall event 77733
Product BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as single unit in thermoformed trays. There are 50 units per case. Product Usage: Vinyl leg bag to be used with male external catheters, Foley catheters, or moth other types of…
Product code KNX
Recalling firm C.R. Bard, Inc.
Recall class Class II
Status Terminated
Termination date Jul 26, 2021
FEI number 1018233

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

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