Recalls / —
—#211292
Product
HUDSON RCI mBrace, ET Tube Holder with Bite Block and 4 Point Head Strap, REF DYNJMBRC4B; tracheal tube fixation device
- FDA product code
- CBH — Device, Fixation, Tracheal Tube
- Device class
- Class 1
- Medical specialty
- Anesthesiology
- Affected lot / code info
- UDI/DI 20193489005339 (case), 10193489005332 (each); All Lots
Why it was recalled
Complaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip which may cause dermal injury depending on the device positioning.
Root cause (FDA determination)
Nonconforming Material/Component
Action the firm took
Medline Industries issued an URGENT MEDICAL DEVICE RECALL to its consignees of 11/18/2024 via USPS and email. The notice explained the issue, risk to user, and requested the destruction of the affected product. For questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.
Recalling firm
- Firm
- MEDLINE INDUSTRIES, LP Northfield
- Address
- 3 Lakes Dr, Northfield, Illinois 60093-2753
Distribution
- Distribution pattern
- US and Canada
Timeline
- Recall initiated
- 2024-11-18
- Posted by FDA
- 2024-12-18
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #211292. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.