MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
Class I - DangerousWhat Should You Do?
- Check if you have this product: GTIN: 0884521128163/ 20884521128160 LOT Numbers: Lot Number 1828200086 1925300170 1925300171 2018800013 2018800024 2018800043 2019500199 2019500200 2019500222 2021000106 2021000107 2029600102 2029600103 2116600083 2131200176 2133700166 2227800108 2230400250 2230400251 2234800071
- 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:
- Covidien LP
- Reason for Recall:
- Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An occluded, partially or fully, and/or uncured or excessive MDX may dislodge from the catheter lead to full catheter obstruction resulting in delay to treatment and partial obstruction resulting in reduced flow, or particulate dislodgement that may result in delay to treatment, hemolysis, embolism/embolus or thrombosis/thrombus
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
Product Codes/Lot Numbers:
GTIN: 0884521128163/ 20884521128160 LOT Numbers: Lot Number 1828200086 1925300170 1925300171 2018800013 2018800024 2018800043 2019500199 2019500200 2019500222 2021000106 2021000107 2029600102 2029600103 2116600083 2131200176 2133700166 2227800108 2230400250 2230400251 2234800071
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2389-2023
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