Device recall

Z-1674-2012: Water Pik Sinusense battery operated device including a blue semi-transparent…

FDA device recall · Class II · Water Pik, Inc.

Key facts

Recall number (Z-number) Z-1674-2012
Recall event 61532
Product Water Pik Sinusense battery operated device including a blue semi-transparent water reservoir, a white hand held button initiated injector device, and a soft seal nozzle affixed to the white injector. The product is sold individually in white, blue red and orange cartons with a photo of the device…
Product code KMA
Recalling firm Water Pik, Inc.
Recall class Class II
Status Terminated
Termination date Aug 7, 2012
FEI number 1712259

At a glance

  • None 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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