Device recall

Z-2949-2026: Cardinal Health Presource Kits: 1) BASIC PACK, Catalog Number: SBA73BPGCA; 2)…

FDA device recall · Class II · Cardinal Health 200, LLC

Key facts

Recall number (Z-number) Z-2949-2026
Recall event 99380
Product Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Catalog Number: SNE11SPHKD; 4) CRANIOTOMY PACK , Catalog Number: SNE12BS01B
Product code OJK
Recalling firm Cardinal Health 200, LLC
Recall class Class II
Status Open, Classified
FEI number 3001236905

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)