Device recall

Z-0466-2025: smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model…

FDA device recall · Class II · Smiths Medical ASD, Inc.

Key facts

Recall number (Z-number) Z-0466-2025
Recall event 95483
Product smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, for use with the CADD-Solis infusion pumps
Product code MEA
Recalling firm Smiths Medical ASD, Inc.
Recall class Class II
Status Open, Classified
510(k) numbers K111275
FEI number 3012307300

At a glance

  • 1–9 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)