Recall
Procedure packs: (1) Presource PBDS Cat. PG33BTO21, Ohio State Univ Wexner Med Ctr, Kit, Roux UH, Sterile; (2) Presource PBDS Cat. PG33BTO22, Ohio State Univ Wexner Med Ctr, Kit, Roux UH, Sterile; (3) Presource PBDS Cat. PG33SROUB, Ohio…
Cardinal Health 200, LLC · 16 Aug 2023
- Status
- Recall open, classified
- Why, in the FDA's words
- “Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).”
- Recall began
- 16 Aug 2023
- Company
- Cardinal Health 200, LLC
- Device type
- Product code (FDE)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.