Pacira Pharmaceuticals, Inc.

FDA Regulatory Profile

Summary

Total Recalls
4
510(k) Clearances
1
Inspections
16
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0567-2024Class IIZilretta (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, June 12, 2024
D-0546-2024Class IIDrug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release injectable suspension), 32 mg pMay 7, 2024
D-0621-2020Class IIEXPAREL, Bupivicaine Liposome Injectable Suspension, 1.3%, 266 mg/20 mL (13 mg/mL), Sterile, 20 mL vNovember 21, 2019
D-168-2013Class IIEXPAREL (bupivacaine liposome injectable suspension), 1.3%, 266 mg/20 mL (13.3 mg/mL) single use viDecember 17, 2012

Recent 510(k) Clearances

K-NumberDeviceDate
K211334Iovera SystemSeptember 10, 2021