Device recall

Z-3179-2011: Olympus Fluid Aspiration Set; a sterile set of silicone tubing and connectors…

FDA device recall · Class II · Northgate Technologies, Inc.

Key facts

Recall number (Z-number) Z-3179-2011
Recall event 59656
Product Olympus Fluid Aspiration Set; a sterile set of silicone tubing and connectors for use with the Olympus SP-2 Fluid Irrigation & Aspiration Pump; 10 sets per box; Manufactured for: Olympus America Inc., Two Corporate Center Drive, Melville, NY 11747-3157; catalog #72-00114-0 The fluid aspiration set…
Product code KQT
Recalling firm Northgate Technologies, Inc.
Recall class Class II
Status Terminated
Termination date Dec 14, 2011
510(k) numbers K921451
FEI number 1450997

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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