Stryker Corporation

Frequent Recalls

7

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-05-20 to 2026-08-12

Date	Source	Product	Brand	Severity	Units
2026-08-12	FDA Device	FDA Recall: STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640	Stryker Corporation	Class II	N/A
2026-06-10	FDA Device	FDA Recall: Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Managem	Stryker Corporation	Class II	N/A
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

Stryker Corporation Recalls | WatchRecall