# FDA recall Z-2452-2024

> **Boston Scientific Corporation** · Class II · device recall initiated 2024-06-27.

## Product

Capio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250.  Capio SLIM Suture Capturing Devices are used by physicians to facilitate the consistent placement of sutures during open surgical procedures.

## Reason for recall

Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.

## Distribution

Domestic: Nationwide Distribution.  International: Pending

## Key facts

- **Recall number:** Z-2452-2024
- **Recalling firm:** Boston Scientific Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-27
- **Report date:** 2024-08-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marlborough, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2452-2024

## Citation

> AI Analytics. FDA recall Z-2452-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-2452-2024. Source: US FDA. Licensed CC0.

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