Stryker recalls FluidSmart Urology Tube Set REF LL0006 with UDI-DI code 00860936000365 due to nonconforming products being inadvertently distributed. Affected units may have safety risks.
Due to nonconforming products being inadvertently distributed.
Stryker is recalling FluidSmart Urology Tube Sets with specific UDI-DI code 00860936000365 because nonconforming products were distributed. This recall is important because the products may not meet safety standards, potentially causing risks during medical procedures.
The recall states that nonconforming products were inadvertently distributed. This means the tube sets might not meet the required safety standards for medical use, which could lead to potential issues during procedures like irrigation or fluid management.
Healthcare professionals using the FluidSmart Urology Tube Sets in urology, gynecology, or orthopedic procedures are most at risk. Patients receiving these tubes during laparoscopic or endoscopic surgeries may be affected.
Check for the product name 'FluidSmart Urology Tube Set', reference code LL0006, and UDI-DI code 00860936000365. These items were distributed with Lot Number B000576601.
Verify the UDI-DI code 00860936000365 and reference number LL0006 on the tube set.
The recall is due to nonconforming products being inadvertently distributed, meaning the tube sets may not meet safety standards.
The official recall notice does not specify a remedy or action steps for affected users.
The recall states nonconforming products were distributed, but the specific risk of injury is not detailed in the official notice.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2166-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2166-2026 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
