Device recall

Z-0796-2020: Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF…

FDA device recall · Class III · Teleflex Medical

Key facts

Recall number (Z-number) Z-0796-2020
Recall event 82307
Product Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500
Product code NNY
Recalling firm Teleflex Medical
Recall class Class III
Status Terminated
Termination date Sep 6, 2023
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

Browse all FDA device recalls (products)