Stephanix recalls D2RS Digital Dynamic Remote System due to potential continued movement after command release, risking unintended motion during medical procedures.
The firm has detected a potential risk using the command. After releasing the command, the movement of the table may continue instead of stopping.
Stephanix is recalling its D2RS Digital Dynamic Remote System because it may continue moving after a command is released. This could cause unintended motion during medical procedures, potentially leading to injury.
The system may continue moving after a command is released, causing unintended motion during medical procedures. This could lead to injury if the movement affects the patient or medical staff.
Medical professionals using the D2RS system for fluoroscopic imaging procedures are most at risk. Patients undergoing vascular angiography or cardiology procedures may also be affected.
The D2RS Digital Dynamic Remote System is used in medical imaging for vascular and cardiology procedures. Check for model numbers DHJ008, DIG010, DIH012, DIH014, DIK022, DIK024, DIL025, DIL030, DJK051, DJK052, DKI032, DKI033, DKJ047, DKK051, DKK052, DLA001, DML062.
Identify the model number on the device, which may be one of DHJ008, DIG010, DIH012, DIH014, DIK022, DIK024, DIL025, DIL030, DJK051, DJK052, DKI032, DKI033, DKJ047, DKK051, DKK052, DLA001, or DML062.
The product may continue moving after a command is released, which could cause unintended motion during medical procedures. Use caution.
Check the model number to see if it is affected. If it is, contact Stephanix for further instructions.
Yes, the system may cause unintended motion during procedures, which could lead to injury.
We’ve drafted a message you can send Stephanix to request your refund or repair — edit it as you like.
Subject: Recall Z-0557-2019 — Stephanix Stephanix Hello, I own a Stephanix that is covered by recall Z-0557-2019 from Stephanix. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
&body=Recall%3A%20Stephanix%20recalls%20STEPHANIX%20D2RS%20Digital%20Dynamic%20Remote%20Systemhttp%3A%2F%2Fcts.fda.gov%2Fdivision-tracking%2Fimages%2Ftrash.png%20Product%20The%20D2RS%0AAgency%3A%20FDA%0ASource%20ID%3A%20Z-0557-2019%0APage%3A%20https%3A%2F%2Fgovinfonow.com%2Frecall%2F69513-stephan-d2rs-digital-dynamic-remote-system-may-continue-moving-after%0A%0AWhat%20looks%20wrong%3A%0A){kind=link}