FDA Device recall Z-0088-2024
Procedure packs: (1) Presource Portacath Pack, Cat
- FDA Device
- Class II
- ongoing
- Published 2023-10-18
On 2023-10-18 the FDA classified a Class II recall of Procedure packs: (1) Presource Portacath Pack, 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-0088-2024 |
| 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 packs: (1) Presource Portacath Pack, Cat. SANV1PIFSB, Medstar Franklin Square Med CE, Sterile; and (2) Presource Bone Marrow Harvest Pack, Cat. SAN12BHGT1, Medstar Georgtown University H, Sterile.
Reason
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Identifiers
| code_info | (1) Cat. SANV1PIFSB - Lot #67711, Exp. 3/1/2026, UDI-DI 10195594532048; and (2) Cat. SAN12BHGT1 - Lot #13526, Exp. 3/1/2024, UDI-DI 10197106202715. |
|---|
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-0088-2024%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.