# FDA recall Z-2632-2023

> **Covidien LP** · Class II · device recall initiated 2023-08-22.

## Product

Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm

## Reason for recall

Some catheter kits labeled as 23 cm implant length incorrectly included catheters of 28 cm implant length; the actual catheter implant length is identifiable based upon the correct labeling on the catheter body.

## Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Brazil, China, Czech Republic, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Portugal, Puerto Rico, Spain, Thailand, United Kingdom.

## Key facts

- **Recall number:** Z-2632-2023
- **Recalling firm:** Covidien LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-22
- **Report date:** 2023-10-04

- **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-2632-2023

## Citation

> AI Analytics. FDA recall Z-2632-2023. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-2632-2023. Source: US FDA. Licensed CC0.

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