TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.
Class I - DangerousWhat Should You Do?
- Check if you have this product: TITAN Operating Tables: 1465166, 1228073, 1397903, 4544260.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Trumpf Medical Systems, Inc.
- Reason for Recall:
- Unintended movement of the operating table during surgical cases due to the use of damaged TITAN remotes.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.
Product Codes/Lot Numbers:
TITAN Operating Tables: 1465166, 1228073, 1397903, 4544260.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0141-2015
Related Recalls
Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions for the purpose of archiving and teaching.
Trumpf Medical Systems
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 has identified six incidents of pinched cables.
Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.