Trumpf Medical recalls surgical camera systems with serial numbers listed that emit excessive radiation, potentially causing hospital equipment to malfunction during surgery. Affected units must be checked by a professional.
The radiated emission from the TruVidia" Wireless Receiver is above the normative accepted limits, in which the radiated emission may interact with other devices in the operating room and cause them not to function properly.
Trumpf Medical is recalling surgical camera systems that emit excessive radiation, which could interfere with other medical devices in the operating room. This poses a risk to surgical safety by potentially causing equipment malfunctions during procedures.
The camera system's wireless receiver emits radiation levels above safety limits. This interference can cause other medical devices in the operating room to malfunction, potentially disrupting critical surgical procedures.
Surgical teams and hospitals using the recalled camera systems are most at risk. Patients undergoing surgery with these devices could experience equipment malfunctions.
Check if your camera system has a serial number listed in the provided list (e.g., 102584474, 102584475, etc.). The product is intended for surgical use and has a catalog number of 1940747.
Verify if your camera system has a serial number from the list provided in the recall notice.
Reach out to Trumpf Medical Systems, Inc. for guidance on next steps if your device is affected.
The wireless receiver emits radiation above safety limits, which may cause other medical devices in the operating room to malfunction.
Check if your serial number is listed in the provided list of numbers (e.g., 102584474, 102584475, etc.).
Contact Trumpf Medical Systems, Inc. for guidance on next steps.
We’ve drafted a message you can send Trumpf Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0824-2018 — Trumpf Medical Trumpf Medical Hello, I own a Trumpf Medical that is covered by recall Z-0824-2018 from Trumpf Medical. 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.
