FDA recall Z-0775-2022

Boston Scientific Corporation · Class II · device

Product

JAGTOME RX 44-30-260-035 Material Number: M00573060

Reason for recall

Sterility of device is compromised due to a sterile barrier breach

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.

Key facts

Status
Ongoing
Initiation date
2021-12-22
Report date
2022-03-23
Voluntary/Mandated
Voluntary: Firm initiated
Location
Marlborough, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0775-2022