Device recall

Z-3118-2026: Products that contain the Pericare Wipes: SureStep" Foley Tray System…

FDA device recall · Class II · C.R. Bard Inc

Key facts

Recall number (Z-number) Z-3118-2026
Recall event 98840
Product Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067 10801741121064 SureStep" Foley Tray System Complete Care Add-A-Foley Catheter REF: A304400A UDI code: 00801741073847 10801741073844 SureStep" Foley Tray System Add-A-Foley…
Product code KNX
Recalling firm C.R. Bard Inc
Recall class Class II
Status Open, Classified
FEI number 1018233

At a glance

  • None 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

Browse all FDA device recalls (products)