Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0090-2024 — Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.

U.S. FDA — Device Enforcement · United States · 2023-08-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0090-2024
Date of alert
2023-08-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10195594542795
Reported risk: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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