JAGTOME RX 39-30-260-025 Material Number: M00573100
Check against the official notice below — it lists the full affected range.
Boston Scientific Corporation has recalled 98 units of the JAGTOME RX 39-30-260-025 medical device (Material Number M00573100) due to a sterile barrier breach that compromises the device's sterility. The affected devices were distributed worldwide, including throughout the United States and in countries including Australia, Canada, China, France, Germany, Japan, the United Kingdom, and many others. The recalled devices are identified by Lot Number 27857328 and GTIN 8714729776529.
The recall notice does not specify a remedy for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
Sterility of device is compromised due to a sterile barrier breach
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 Quantity: 98 units Lot/code info: Lot Numbers: 27857328 GTIN: 8714729776529
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.