Bard Brachytherapy, Inc.

FDA Regulatory Profile

Bard Brachytherapy, Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1702-2018, Class II) was initiated on April 10, 2018.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
3
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1702-2018Class IIBARD¿ BrachySource¿ Iodine125 radioactive seeds consist of a welded titanium capsule containing the April 10, 2018