PlainRecalls
FDA Devices Moderate Class II Ongoing

DREAMTOME 49-30MM/260CM Material Number: M00584010

Reported: March 23, 2022 Initiated: December 22, 2021 #Z-0757-2022

Product Description

DREAMTOME 49-30MM/260CM Material Number: M00584010

Reason for Recall

Sterility of device is compromised due to a sterile barrier breach

Details

Units Affected
472 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.
Location
Marlborough, MA

Frequently Asked Questions

What product was recalled?
DREAMTOME 49-30MM/260CM Material Number: M00584010. Recalled by Boston Scientific Corporation. Units affected: 472 units.
Why was this product recalled?
Sterility of device is compromised due to a sterile barrier breach
Which agency issued this recall?
This recall was issued by the FDA Devices on March 23, 2022. Severity: Moderate. Recall number: Z-0757-2022.