Device recall

Z-0754-2017: HF Cable WA00014A, Endoscopic electrosurgical unit and accessories

FDA device recall · Class II · Olympus Corporation of the Americas

Key facts

Recall number (Z-number) Z-0754-2017
Recall event 75601
Product HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
Product code FAS
Recalling firm Olympus Corporation of the Americas
Recall class Class II
Status Terminated
Termination date Feb 6, 2019
510(k) numbers K120418
FEI number 2429304

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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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