Z-2725-2026 Class II Ongoing

Recalled by Boston Scientific Corporation — Marlborough, MA

FDA device recall Z-2725-2026 was initiated by Boston Scientific Corporation on June 30, 2026 and is designated Class II. 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 com… The recall status is ongoing. Affected quantity: 153,921 (US); 119,274 (OUS).

Recall Details

Product Type
Devices
Report Date
July 22, 2026
Initiation Date
June 30, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
153,921 (US); 119,274 (OUS)

Product Description

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 Pattern

US Nationwide distribution. OUS consignee list pending.

Code Information

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