# FDA recall Z-1699-2023

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

## Product

Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF 50816G, e) REF 50818G, f) REF 53810G, g) REF 53812G, h) REF 53814G, i) REF 53816G, j) REF 53818G, k) REF 53820G

## 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-1699-2023
- **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-1699-2023

## Citation

> AI Analytics. FDA recall Z-1699-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1699-2023. Source: US FDA. Licensed CC0.

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