Device recall

Z-0844-2011: Fresenius Medical CombiSet BVM Hemodialysis Blood Tubing Set P/N: 03-2795-7

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

Key facts

Recall number (Z-number) Z-0844-2011
Recall event 57293
Product Fresenius Medical CombiSet BVM Hemodialysis Blood Tubing Set P/N: 03-2795-7
Product code FJK
Recalling firm Fresenius Medical Care Holdings, Inc.
Recall class Class I
Status Terminated
Termination date Nov 3, 2012
510(k) numbers K962081
FEI number 3001451489

At a glance

  • 1–9 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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