Device recall

Z-0087-2024: Procedure packs: (1) Presource PBDS, Cat. PGMHSUESR, Southeast Hospital MHHS…

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

Key facts

Recall number (Z-number) Z-0087-2024
Recall event 92875
Product Procedure packs: (1) Presource PBDS, Cat. PGMHSUESR, Southeast Hospital MHHS, Kit, Set Up No Drape, SE, Sterile; (2) Presource PBDS Cat. PGVGLBP20, Parkview Medical Center, Kit, Lap Chole, Sterile; (3) Presource PBDS Cat. PG63CCC31, USPI Christ Hosp Spine Srgry C, Kit, Basic, Sterile; (4) Presource…
Product code LRO
Recalling firm Cardinal Health 200, LLC
Recall class Class II
Status Open, Classified
FEI number 3001236905

At a glance

  • None Linked 510(k)s
  • 10–99 Products in the same recall event
  • 1,000+ 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)