Device recall

Z-2831-2011: Rusch, Sure Seal Golden Drain, One Piece Urinary Incontinence Device, Teleflex…

FDA device recall · Class II · Teleflex Medical

Key facts

Recall number (Z-number) Z-2831-2011
Recall event 59184
Product Rusch, Sure Seal Golden Drain, One Piece Urinary Incontinence Device, Teleflex Medical. Used for urine collection.
Product code NNY
Recalling firm Teleflex Medical
Recall class Class II
Status Terminated
Termination date Mar 20, 2012
FEI number 3005747797

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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