LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF# e2400-51

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number/Exp. Date: RED1752 2018-12 RED1758 2019-01 RED1772 2019-06
  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:
LeMaitre Vascular, Inc.
Reason for Recall:
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF# e2400-51

Product Codes/Lot Numbers:

Lot Number/Exp. Date: RED1752 2018-12 RED1758 2019-01 RED1772 2019-06

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1443-2017

Related Recalls

Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.

Aug 25, 2025 Other Medical Devices View Details →