Effectively Manage Medical Device Recalls, Field Actions, and Alerts
Software defects and sterility issues remain among the leading causes of medical device recalls, field actions, and alerts. Class I recalls — the FDA’s highest-risk designation — carry significant regulatory exposure when supply chain notification isn’t fully documented.
TRIEVR Recall is an on-demand SaaS platform that replaces manual, error-prone notification and tracking with a documented, auditable workflow — including FDA reporting tools to help your team compile and submit required regulatory information.

Manual Recall Processes Create Regulatory and Legal Exposure
Phone trees, spreadsheets, and email chains are not an audit trail. When the FDA reviews your recall execution, they will examine every communication, every timestamp, and every non-response.
TRIEVR replaces ad hoc manual processes with a structured, documented workflow purpose-built for regulatory defensibility — at a fraction of the cost of legacy QMS platforms. Our SaaS platform can have your recall underway in minutes.
Enterprise-Grade Recall Execution
+ Platform Features
Progress Dashboard
Our platform also Includes:

+ Additional Options
Fast. Documented. Defensible.
TRIEVR ensures every cosmetic recall is executed efficiently, documented completely, and aligned with your regulatory obligations. On-demand access means you pay only for active use — no monthly fees, no annual contracts, no cost between recalls.
Fast. Documented. Defensible.
TRIEVR ensures every cosmetic recall is executed efficiently, documented completely, and aligned with your regulatory obligations. On-demand access means you pay only for active use — no monthly fees, no annual contracts, no cost between recalls.



