HIGH

B Braun Medical Recalls Anesthesia Tray Over Connector Hazard

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.

Quick Facts at a Glance

Recall Date
September 18, 2025
Hazard Level
HIGH
Brand
B BRAUN MEDICAL
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Potential for the lid of the catheter connector to be in the incorrect position.

What You Should Do

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

Product Details

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 Hazard

The issue relates to the lid of the catheter connector potentially being in the incorrect position. This defect can lead to improper anesthesia administration.

Reported Incidents

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.

What to Do

Patients and healthcare providers should stop using the device immediately. Follow the recall instructions and contact B Braun Medical for further guidance.

Contact Information

For more information, contact B Braun Medical Inc. Visit their website or call customer service for assistance.

Key Facts

  • Recall date: September 18, 2025
  • Product code: NES1727KFX
  • Total units recalled: 2,840
  • Hazard classification: Class II
  • Affected states: Nationwide distribution
View Original Recall on FDA - Medical Devices

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeAnesthesia Tray
Sold At
Multiple Retailers

Product Details

Model Numbers
NES1727KFX
REF: 333197
UDI-DI (Primary): 04046964179327
UDI-DI (Unit of Use): 04046964179310
Lot Numbers: 0062000732
+1 more
Affected States
ALL
Report Date
October 15, 2025
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE

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