Device recall

Z-2467-2010: Braun wheelchair lift, model NL, Braun Corporation, Winamac, IN A wheelchair…

FDA device recall · Class II · The Braun Corporation

Key facts

Recall number (Z-number) Z-2467-2010
Recall event 56686
Product Braun wheelchair lift, model NL, Braun Corporation, Winamac, IN A wheelchair lift for motor vehicles.
Product code ING
Recalling firm The Braun Corporation
Recall class Class II
Status Terminated
Termination date May 12, 2011
510(k) numbers K952946
FEI number 1827452

At a glance

  • 1–9 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)