FDA Device recall Z-1416-2025
Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204
- FDA Device
- Class II
- ongoing
- Published 2025-04-02
On 2025-04-02 the FDA classified a Class II recall of Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204 by Baxter Healthcare, citing there is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1416-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-02-25 |
| Published | 2025-04-02 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204
Reason
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Identifiers
| code_info | UID/DI 00887761974326, All serial numbers manufactured until 11/14/2024. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1416-2025%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.