FDA recall D-0741-2022

Vitae Enim Vitae Scientific, Inc. · Class II · drug

Product

TETRACAINE 1% Tetracaine HCI Injection, USP, 20mg/2mL (10mg/mL), 10 x 2ml Single Use Vials per box, Rx only, Manufactured for Cameron Pharmaceuticals, LLC., NDC 42494-437-10.

Reason for recall

Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.

Distribution

Nationwide in the U.S.A

Key facts

Status
Terminated
Initiation date
2022-03-14
Report date
2022-04-13
Termination date
2024-08-15
Voluntary/Mandated
Voluntary: Firm initiated
Location
San Diego, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0741-2022