Device recall

Z-1639-2014: Naturalyte Liquid Bicarbonate Concentrate, 6.4 Liter Bottle Part Number…

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

Key facts

Recall number (Z-number) Z-1639-2014
Recall event 67922
Product Naturalyte Liquid Bicarbonate Concentrate, 6.4 Liter Bottle Part Number: 08-4000-LB The concentrate is formulated to be used with a three steam hemodialysis machine which is calibrated for acid and bicarbonate concentrates
Product code KPO
Recalling firm Fresenius Medical Care Holdings, Inc.
Recall class Class I
Status Open, Classified
510(k) numbers K071387
FEI number 3001451489

At a glance

  • 1–9 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

Browse all FDA device recalls (products)