Revive Rx LLC dba Revive Rx Pharmacy

FDA Regulatory Profile

Revive Rx LLC dba Revive Rx Pharmacy appears in FDA public data with 3 recalls — including 2 Class I (most serious) —, 0 510(k) clearances, 3 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0511-2024, Class I) was initiated on April 20, 2024.

Summary

Total Recalls
3 (2 Class I)
510(k) Clearances
0
Inspections
3
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0511-2024Class ITirzepatide 10 mg/0.5 mL Sterile Solution, 2 mL Multi-dose vial, Rx only, This is a Compounded ProduApril 20, 2024
D-0771-2023Class IITirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial, Rx Only, For Sub-Q Use Only, Compounded Drug PrMay 11, 2023
D-0648-2022Class IHCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV Use, Vial,February 11, 2022