LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Number/Exp. Date: RED1743 2018-09 RED1744 2018-09 RED1749 2018-10 RED1750 2018-12 RED1751 2018-12 RED1755 2018-12 RED1756 2018-12 RED1757 2019-01 RED1759 2019-02 RED1760 2019-02 RED1761 2019-03 RED1764 2019-03 RED1766 2019-04 RED1767 2019-04 RED1768 2019-05 RED1769 2019-05 RED1771 2019-06 RED1773 2019-07 RED1774 2019-07 RED1775 2019-07
- 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:
- 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 Catheter (eIFU) REF# e2400-50
Product Codes/Lot Numbers:
Lot Number/Exp. Date: RED1743 2018-09 RED1744 2018-09 RED1749 2018-10 RED1750 2018-12 RED1751 2018-12 RED1755 2018-12 RED1756 2018-12 RED1757 2019-01 RED1759 2019-02 RED1760 2019-02 RED1761 2019-03 RED1764 2019-03 RED1766 2019-04 RED1767 2019-04 RED1768 2019-05 RED1769 2019-05 RED1771 2019-06 RED1773 2019-07 RED1774 2019-07 RED1775 2019-07
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1442-2017
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Labeling mix-up resulting in the incorrect lot outer packaging of product.
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The device was incorrectly packed in the wrong size labeled outer packaging.
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.