# FDA recall Z-2725-2026

> **Boston Scientific Corporation** · Class II · device recall initiated 2026-06-30.

## Product

Rapid Refill Continuous Injection System, UPN M00566001

## Reason for recall

Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loose connection or complete disconnection. May lead to difficulty connecting syringe, inability to aspirate or inject properly, fluid leakage, or separation of the syringe from the system, potentially requiring device exchange and prolonging the procedure.

## Distribution

US Nationwide distribution. OUS consignee list pending.

## Key facts

- **Recall number:** Z-2725-2026
- **Recalling firm:** Boston Scientific Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-30
- **Report date:** 2026-07-22

- **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-2725-2026

## Citation

> AI Analytics. FDA recall Z-2725-2026. Retrieved 2026-09-21 from https://api.ai-analytics.org/recall/Z-2725-2026. Source: US FDA. Licensed CC0.

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