Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Boston Scientific Zurpaz(TM) MEDIUM CURL Recalled by Creganna Medical Devices Due to Lack of sterility assurance.

Date: May 22, 2017
Company: Creganna Medical Devices
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Creganna Medical Devices directly.

Affected Products

Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USTMCA85200

Quantity: 85 units

Why Was This Recalled?

Lack of sterility assurance.

Where Was This Sold?

This product was distributed to 1 state: MA

Affected (1 state)Not affected

About Creganna Medical Devices

Creganna Medical Devices has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report