Lundbeck LLC

FDA Regulatory Profile

Lundbeck LLC appears in FDA public data with 1 recall, 0 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1142-2023, Class III) was initiated on August 17, 2023.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1142-2023Class IIISabril (vigabatrin) for Oral Solution, 500 mg, 50 Packets, Rx only, Manufactured by: Patheon, CincinAugust 17, 2023