FDA Device recall Z-2293-2025
High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C
- FDA Device
- Class II
- ongoing
- Published 2025-08-20
On 2025-08-20 the FDA classified a Class II recall of High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C by Merit Medical Systems, citing high pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may res….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2293-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-06-05 |
| Published | 2025-08-20 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Merit Medical Systems |
| Distribution | US |
Product
High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C
Reason
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
Identifiers
| code_info | REF/UDI-DI/Lot(Expiration): 502211002/I3116954(8/16/2028); HP9720E/C/00884450859889/I3116059(12/10/2027), I3127321(12/3…REF/UDI-DI/Lot(Expiration): 502211002/I3116954(8/16/2028); HP9720E/C/00884450859889/I3116059(12/10/2027), I3127321(12/30/2027), I3137220(1/28/2028); HP9721E/C/00884450859896/I3116060(12/10/2027) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2293-2025%22
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