FDA Device recall Z-0085-2024
Procedure pack: Presource PBDS, Cat
- FDA Device
- Class II
- ongoing
- Published 2023-10-18
On 2023-10-18 the FDA classified a Class II recall of Procedure pack: Presource PBDS, Cat by Cardinal Health 200, citing packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0085-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-08-16 |
| Published | 2023-10-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cardinal Health 200 |
| Distribution | US |
Product
Procedure pack: Presource PBDS, Cat. PEMHEEESR, Southeast Hospital MHHS, Kit, ENT, SE, Sterile.
Reason
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Identifiers
| code_info | Lot #967679, Exp. 9/1/2024, UDI-DI 10195594543259. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0085-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.