Device recall

Z-0117-2007: Abbott AxSYM Matrix Cells--Product List No: 8A73-02, sold in boxes of 100

FDA device recall · Class II · Abbott Diagnostic International, Ltd.

Key facts

Recall number (Z-number) Z-0117-2007
Recall event 36417
Product Abbott AxSYM Matrix Cells--Product List No: 8A73-02, sold in boxes of 100
Product code JJE
Recalling firm Abbott Diagnostic International, Ltd.
Recall class Class II
Status Terminated
Termination date Jan 24, 2012
510(k) numbers K041811, K974651
FEI number 2623532

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

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