Device recall

Z-0355-2007: TraXis Fixed Rasp in sizes: 7mm, 9mm, 11mm, 13mm and 15mm; for use with TraXis…

FDA device recall · Class II · Abbott Spine

Key facts

Recall number (Z-number) Z-0355-2007
Recall event 36731
Product TraXis Fixed Rasp in sizes: 7mm, 9mm, 11mm, 13mm and 15mm; for use with TraXis vertebral body replacement system
Product code MQP
Recalling firm Abbott Spine
Recall class Class II
Status Terminated
Termination date Oct 11, 2007
510(k) numbers K060841
FEI number 3000718496

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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