Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Perfector Product Usage: Muscle stimulation

FDA Recall Z-1137-2012 · Posted 2012-03-01

Recalling FirmIon Genius, Inc.
Recall StatusTerminated
Product CodeIPF
Date Initiated2012-01-06
Date Terminated2015-05-21
Product Quantity72 cables in total, amounts of other devices not reported

Reason for Recall

Wires do not meet performance standards under 21 CFR 898 and have unprotected electrode configurations. Additionally, devices were sold/distributed without 510(k) or PMA

Firm Action

Ion Genius sent a Medical Device Product Recall letters to all affected customers on January 6, 2012. The letter identified the affected products, problem and actions to be taken. The letter instructed customers to check their inventory for the affected products and return immediately to Ion Genius for replacements. Customers returning affected products should call the firm so that a shipping label can be provided. Customers were instructed to be completed the Response Form and returned to Ion Genius by fax at 808-395-0787. For questions and concerns contact Xanya Sofra-Weiss at 808-222-2664 or email [email protected].

Root Cause

Nonconforming Material/Component

Distribution Pattern

Worldwide Distribution - (USA) Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑