# FDA recall Z-0877-2023

> **Covidien LP** · Class I · device recall initiated 2022-12-07.

## Product

MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only:     13.5cm, Straight Extensions, Kit - Model No. 8888135131;   13.5 cm, Curved Extensions, Kit - Model No. 8888135132;   13.5cm, Pre-Curved, Kit - Model No. 8888135133;   13.5cm, Straight Extensions, IC Tray, Model No. 8888135134;     16cm, Straight Extensions, Kit - Model No. 8888135161;   16cm, Curved Extensions, Kit - Model No. 8888135162;   16 cm, Pre-Curved, Kit - Model No. 8888135163;   16cm, Straight Extensions, IC Tray - Model No. 8888135164;     19.5cm, Straight Extensions, Kit - Model No. 8888135191;   19.5cm, Curved Extensions, Kit - Model No. 8888135192;   19.5cm, Pre-Curved, Kit - Model No. 8888135193;   19.5cm, Straight Extensions, IC Tray - Model No. 8888135194;   19.5cm, Curved Extensions, PASS Tray - Model No. 8888135198;     24cm, Straight Extensions, Kit - Model No. 8888135241;   24cm, Curved Extensions, Kit - Model No. 8888135242;   24cm, Pre-Curved, Kit - Model No. 888813524

## Reason for recall

There is a potential leaking condition within the hub of affected devices, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return during use.

## Distribution

Worldwide distribution. US nationwide including Guam, USVI, and Puerto Rico;  Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Costa Rica, Czech Republic, Denmark, Dominican Republic, Ecuador, Finland, France, French Polynesia, Germany, Greece, Hungary, Iceland, Italy, Jamaica, Kenya, Malaysia, Malta, Mauritius, Mexico, Nicaragua, Norway, Oman, Panama, Peru, Philippines, Poland, Portugal, Romania, Russian Federation, Saudi Arabia, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Trinidad And Tobago, Tunisia, Turkey, Uganda, United Arab Emirates, and United Kingdom.

## Key facts

- **Recall number:** Z-0877-2023
- **Recalling firm:** Covidien LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-07
- **Report date:** 2023-01-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0877-2023

## Citation

> AI Analytics. FDA recall Z-0877-2023. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-0877-2023. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*