DREAMTOME 49-30MM/450CM Material Number: M00584030

FDA Recall #Z-0758-2022 — Class II — December 22, 2021

Recall #Z-0758-2022 Date: December 22, 2021 Classification: Class II Status: Ongoing

Product Description

DREAMTOME 49-30MM/450CM Material Number: M00584030

Reason for Recall

Sterility of device is compromised due to a sterile barrier breach

Recalling Firm

Boston Scientific Corporation — Marlborough, MA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

32 units

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, Botswana, China, Czech Republic, Denmark, Finland, France, Germany, Great Britain, Greece, Ireland, Italy, Japan, Korea, Kuwait, Latvia, Lebanon, Mauritius, Morocco, Namibia, Netherlands, New Zealand, Norway, Poland, Portugal, Qatar, Romania, Russian Fed., Saudi Arabia, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Unit. Arab Emir.

Code Information

Lot Numbers: 27692922 GTIN: 8714729778257

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated