FDA Device recall Z-2389-2023
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
- FDA Device
- Class I
- ongoing
- Published 2023-08-23
On 2023-08-23 the FDA classified a Class I recall of MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP by Covidien, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2389-2023 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-06-28 |
| Published | 2023-08-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Covidien |
| Distribution | US |
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
Reason
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
Identifiers
| code_info | GTIN: 0884521128163/ 20884521128160 LOT Numbers: Lot Number 1828200086 1925300170 1925300171 2018800013 2018800024 201…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2389-2023%22
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