ENDOMAGNETICS LTD: Device Recall
Recall #Z-0316-2026 · 10/01/2025
Class II: Risk
Recall Details
- Recall Number
- Z-0316-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- ENDOMAGNETICS LTD
- Status
- Ongoing
- Date Initiated
- 10/01/2025
- Location
- Cambridge, N/A, United Kingdom
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,760 units
Reason for Recall
Potential for contamination with cotton fibers.
Product Description
Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for use to radiographically mark soft tissue during a surgical procedure or for future surgical procedures.
Distribution Pattern
Worldwide - US Nationwide distribution in the states of CA, CO, CT, DC, FL, GA, IA, ID, IN, KY, MD, ME, MI, MN, MO, NC, ND, NE, NH, NJ, NY, OH, TX, WA and the country of Canada.
Other Recalls by ENDOMAGNETICS LTD
- Class II: Risk 10/01/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.