Recall Z-0090-2024— Cardinal Health 200, LLC
Class II · Ongoing
Class II FDA medical device recall by Cardinal Health 200, LLC, initiated 2023-08-16. FDA's recall record names no specific 510(k) clearance for this event. Product: Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.. Reason: Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits)..
- Recalling firm
- Cardinal Health 200, LLC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-08-16
- Firm location
- Waukegan, IL, United States
Product description
Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.
Reason for recall
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Data sourced from openFDA. This site is unofficial and independent of the FDA.