Stryker Corporation
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-05-20 to 2026-05-20
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-05-20 | FDA Device | FDA Recall: Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube | Stryker Corporation | Class II | N/A |