Device recall

Z-0490-2014: Nephros Dual Stage Ultra Filter (DSU) Brochure Document 60-3003 Revisions: 0, 1…

FDA device recall · Class I · Nephros Inc

Key facts

Recall number (Z-number) Z-0490-2014
Recall event 66735
Product Nephros Dual Stage Ultra Filter (DSU) Brochure Document 60-3003 Revisions: 0, 1, 2 Product Usage: A disposable point of use water ultrafilter that delivers microbiologically pure water for washing and drinking.
Recalling firm Nephros Inc
Recall class Class I
Status Terminated
Termination date Jul 6, 2016
FEI number 3003337893

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event

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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