🔍 RecallPedia

CE17TFC CONTINUOUS EPID SET W/17G TUOHY, Material Number 332238 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?

  1. Check if you have this product:
    Batch: 61590460, 61594135, 61598572, 61601772, 61605134, 61610126, 61613471, 61615656, 61618348, 61621766
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:

CE17TFC CONTINUOUS EPID SET W/17G TUOHY, Material Number 332238 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: 61590460, 61594135, 61598572, 61601772, 61605134, 61610126, 61613471, 61615656, 61618348, 61621766

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3374-2018

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