# FDA recall Z-1701-2023

> **C.R. Bard Inc** · Class II · device recall initiated 2023-04-20.

## Product

HydroSil Go Intermittent Urinary Catheters, Catalog Numbers:  a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818

## Reason for recall

Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-1701-2023
- **Recalling firm:** C.R. Bard Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-20
- **Report date:** 2023-06-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Covington, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1701-2023

## Citation

> AI Analytics. FDA recall Z-1701-2023. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1701-2023. Source: US FDA. Licensed CC0.

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