🔍 RecallPedia

PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFCPS. Product Description: CE17TKFCPS EPIDURAL FULL TRAY.

Class I - Dangerous
🏥 Medical Devices Recalled: September 18, 2025 B BRAUN MEDICAL Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    REF: 332078; Product Code: CE17TKFCPS; UDI-DI (Primary): 04046955899432; UDI-DI (Unit of Use): 04046955899449; Lot Numbers: 0062006314, 0062011670, 0062028428. Expiration Date: 07/31/2026
  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:
Potential for the lid of the catheter connector to be in the incorrect position.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFCPS. Product Description: CE17TKFCPS EPIDURAL FULL TRAY.

Product Codes/Lot Numbers:

REF: 332078; Product Code: CE17TKFCPS; UDI-DI (Primary): 04046955899432; UDI-DI (Unit of Use): 04046955899449; Lot Numbers: 0062006314, 0062011670, 0062028428. Expiration Date: 07/31/2026

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0115-2026

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