HERON THERAPEUTICS, INC.

FDA Regulatory Profile

HERON THERAPEUTICS, INC. appears in FDA public data with 1 recall, 0 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1335-2022, Class III) was initiated on August 2, 2022.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
4
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1335-2022Class IIIZynrelef (bupivacaine and meloxicam), 400 mg bupivacaine and 12 mg meloxicam single dose applicationAugust 2, 2022