# FDA recall Z-2372-2021

> **Covidien, LP** · Class II · device recall initiated 2021-05-28.

## Product

Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 28 cm, Item Code 8888541028P

## Reason for recall

This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-2372-2021
- **Recalling firm:** Covidien, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-05-28
- **Report date:** 2021-09-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** North Haven, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2372-2021

## Citation

> AI Analytics. FDA recall Z-2372-2021. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2372-2021. Source: US FDA. Licensed CC0.

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