Device recall

Z-0398-2018: OSCILLATING SAW ATTACHMENT Surgical instrument motors and…

FDA device recall · Class II · The Anspach Effort, Inc.

Key facts

Recall number (Z-number) Z-0398-2018
Recall event 78901
Product OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical procedures to cut hard tissue or bone and soft tissue.
Product code HWE
Recalling firm The Anspach Effort, Inc.
Recall class Class II
Status Terminated
Termination date Jul 30, 2019
FEI number 1045834

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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