B Braun Medical recalled 2,840 anesthesia trays on September 18, 2025. The recall stems from a potential defect in the catheter connector lid position. The product poses a high hazard risk to patients and healthcare providers.
Potential for the lid of the catheter connector to be in the incorrect position.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact B BRAUN MEDICAL INC or your healthcare provider for instructions. Notification method: Letter
The recall involves the Combined Spinal and Epidural Anesthesia Tray, model NES1727KFX. It distributed nationwide to multiple states including California, Texas, and Florida. The product code is NES1727KFX.
The issue relates to the lid of the catheter connector potentially being in the incorrect position. This defect can lead to improper anesthesia administration.
There are no reported injuries or deaths associated with this recall at this time. The product recall is classified as Class II due to the potential risk.
Patients and healthcare providers should stop using the device immediately. Follow the recall instructions and contact B Braun Medical for further guidance.
For more information, contact B Braun Medical Inc. Visit their website or call customer service for assistance.
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