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Stryker Corporation

Stryker Corporation: 4 recalls listed since February 2026 across FDA.

By year

  • 20264

By agency

  • FDA4

By category

  • Medical Device4

All recalls (4)

Stryker Ahto Tube Sets and Suction/Irrigator Packaging

Stryker tube sets can leak from the handpiece during use.

Moderate risk, FDA, , Device defect

Neptune Smart Docking Station

The Neptune Smart Docking Station may not have completed required testing and poses a risk of electrical shock.

Moderate risk, FDA, , Device defect

Thermedx FluidSmart Urology Tube Set

Due to nonconforming products being inadvertently distributed.

Moderate risk, FDA, , Device defect

Stryker MOLLI 2 System, Introducers, Wand, OncoPen and Tablet

The Molli 2 System needs updated labeling because magnetized surgical tools can dislodge markers during tissue removal.

Moderate risk, FDA, , Labeling error
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