Device recall

Z-1736-2010: EVA 450 Patient Lift Battery Charger.

FDA device recall · Class II · Romedic, Inc.

Key facts

Recall number (Z-number) Z-1736-2010
Recall event 55659
Product EVA 450 Patient Lift Battery Charger.
Product code FSA
Recalling firm Romedic, Inc.
Recall class Class II
Status Terminated
Termination date Sep 30, 2010
FEI number 3008284642

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 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)