US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 19, 2019 (7 years ago)

Procaine HCL

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility

What was recalled

PROCAINE HCL (PFV) 20 MG/ML INJECTABLE SOLUTION, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0900-30

Recalling firm
RXQ Compounding LLC
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1697-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Procaine recalls

See all
Class II · Moderate risk Ongoing

Procaine HCL 2%

Reason Lack of Assurance of Sterility

TMC Acquisition LLC dba Tailor Made Compounding D-1222-2022
Class II · Moderate risk Terminated

S-Procaine HCL 2% Buffered

Reason Lack of Assurance of Sterility

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy D-0279-2020
Class II · Moderate risk Terminated

S-Procaine HCL 1% Buffered Mdv

Reason Lack of Assurance of Sterility

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy D-0245-2020
Class II · Moderate risk Terminated

Procaine HCL 8%

Reason Lack of Assurance of Sterility

RXQ Compounding LLC D-1698-2019