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, the most serious class), 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 Apr 20, 2024. Its most recent FDA inspection ended on Feb 7, 2025 (Official Action Indicated (OAI)).

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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…Apr 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…May 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…Feb 11, 2022

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 7, 2025Houston, TXDrugsOfficial Action Indicated (OAI)3016710945
May 4, 2022Houston, TXDrugsVoluntary Action Indicated (VAI)3016710945
Aug 6, 2021Houston, TXDrugsOfficial Action Indicated (OAI)3016710945

FDA Data Dashboard classifications: NAI (no action indicated), VAI (voluntary action indicated), OAI (official action indicated).