Stryker Corporation recalls

8 recalls.

• STRYKER PKG. recall (Stryker Corporation)
  Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
• STRYKER PKG. recall (Stryker Corporation)
  Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
• STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING recall (Stryker Corporation)
  Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
• STRYKER AHTO TUBE SET WITH TIP PACKAGING recall (Stryker Corporation)
  Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
• STRYKER AHTO TUBE SET PACKAGING recall (Stryker Corporation)
  Medical deviceClass IIReported August 12, 2026 · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
• Neptune Smart Docking Station recall (Stryker Corporation)
  Medical deviceClass IIReported June 10, 2026 · It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required...
• Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The... recall (Stryker Corporation)
  Medical deviceClass IIReported May 20, 2026 · Due to nonconforming products being inadvertently distributed.
• MOLLI 2 System System includes: MM1000 recall (Stryker Corporation)
  Medical deviceClass IIReported February 25, 2026 · Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target...