Device recall

Z-0920-2014: Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine Part…

FDA device recall · Class II · Fresenius Medical Care Holdings, Inc.

Key facts

Recall number (Z-number) Z-0920-2014
Recall event 66953
Product Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine Part Number: 650103. The adapter is a socket that accepts the 2008 machine spike to draw concentrate from the container.
Product code KDI
Recalling firm Fresenius Medical Care Holdings, Inc.
Recall class Class II
Status Terminated
Termination date May 18, 2021
FEI number 3001451489

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 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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