# FDA recall Z-1276-2021

> **Epimed International, Inc.** · Class II · device recall initiated 2021-02-01.

## Product

Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter  Catalog #: 157-1924     Intended for epidural anesthesia and is limited to placement of 72 hours or less

## Reason for recall

Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off

## Distribution

US Nationwide distribution

## Key facts

- **Recall number:** Z-1276-2021
- **Recalling firm:** Epimed International, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-02-01
- **Report date:** 2021-03-24
- **Termination date:** 2022-10-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Johnstown, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1276-2021

## Citation

> AI Analytics. FDA recall Z-1276-2021. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-1276-2021. Source: US FDA. Licensed CC0.

---

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