ES1827K SPINAL/EPIDURAL TRAY (LF), Material Number 333192 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

Class I - Dangerous

🏥 Medical Devices Recalled: July 20, 2018 B. Braun Medical Surgical Instruments Nationwide

What Should You Do?

Check if you have this product:
Batch: 61592518, 61600751, 61596330, 61603763, 61608873, 61612141, 61615216, 61619581, 61617800, 61621835
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:: B. Braun Medical, Inc.
Reason for Recall:: The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: terminated

Product Information

Full Description:

ES1827K SPINAL/EPIDURAL TRAY (LF), Material Number 333192 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

Product Codes/Lot Numbers:

Batch: 61592518, 61600751, 61596330, 61603763, 61608873, 61612141, 61615216, 61619581, 61617800, 61621835

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3391-2018

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