For modern hospital compliance teams

Supply chain resiliency,
redefined

RecCheckMD is the modern platform hospital compliance teams use to detect every recall hitting their supply chain, manage the response with a structured workflow, and produce audit-ready documentation — all in one place.

68,670
FDA Recalls Indexed
82,165
Product Codes Mapped
< 2 min
Time to Results
What RecCheckMD Does
A complete recall response platform

Five integrated capabilities — from the moment a PO hits the system to the moment a JC surveyor signs off. No bolt-on tools, no manual hand-offs.

01

Detect

Match every PO against 68,670+ FDA recalls. Confidence-tiered scoring catches clean catalog hits and fuzzier matches alike.

Hourly openFDA refresh · Device + Drug
02

Triage

Alerts ranked by FDA recall class — Class I at the top. Bulk operations let your team clear backlogs in one click.

Class I / II / III · Bulk review
03

Resolve

Structured JC workflow: New → Under Review → Action Taken → Resolved. Track disposition, notifications, and patient impact per alert.

JC-aligned states · Audit log · Dept routing
04

Track

Vendor scorecards turn recall data into procurement intelligence. See risk trends and inform renewals with hard data.

Per-firm risk · 6-month sparklines
05

Prove

Audit-ready PDF reports per alert. Every PO preserved in encrypted storage. Timestamped attribution on every change — the paper trail JC surveyors expect.

Per-alert PDFs · Encrypted archive
AI Assistant included

Ask anything about your supply chain.

Every RecCheckMD account includes an AI assistant that knows your alerts, vendors, compliance status, and history. Ask it questions in plain English — get answers backed by your own data.

  • "Which Medtronic devices in my inventory have unresolved Class I recalls?"
  • "What's my compliance score, and which alerts are most overdue?"
  • "Show me the top three vendors by recall volume this quarter."
  • "Estimate spend at risk across all unresolved alerts."

Powered by Claude. Trained on RecCheckMD's full data model. Available on every page, every device.

Why this matters

The recall response gap is real — and it's where patients get hurt.

4,000+
FDA device recalls per year
70%
of hospitals still check manually
Hourly
openFDA monitoring with us
< 2 min
upload to prioritized list
Result Grouping
How results are ranked

Results are grouped first by FDA recall class — the severity level FDA assigns to each recall — then within each class, sorted by match confidence. Class I always sits at the top of the report.

Class I

Most serious

Reasonable probability of serious adverse health consequences or death. Always appears at the top of the report. A Class I match with strong confidence triggers a "Stop Use" recommendation and a push notification.

Class II

Moderate severity

May cause temporary or medically reversible adverse health consequences. Remote probability of serious consequences. Reviewed after Class I; handle according to the recommended action on each line.

Class III

Low severity

Unlikely to cause adverse health consequences but violates FDA law or regulation. Usually labeling or documentation issues. Lowest priority on the report but still worth tracking for compliance records.

Within Each Class

Sorted by match confidence

Every matched line gets a score from 0 to 1 based on how well your catalog number, manufacturer, and description line up with the recall. Within each class group, higher-confidence matches appear first.

Score 0.85+
Confident match
Catalog number hit a labeled product code in the recall and the manufacturer lined up. Reliable for clinical action.
Score 0.50–0.84
Likely match
Partial supporting evidence — manufacturer overlap or description similarity. Usually real but worth a human glance.
Score <0.50
Possible match
Number appears in recall text without labeled-code or manufacturer confirmation. Requires manual verification.
Supported Formats
Upload what you already have

Export from your ERP, your spend analytics tool, or any spreadsheet. As long as the required columns are present, RecCheckMD will read it.

XLSX

Excel workbook

First sheet is read. Headers on the first row. Multi-row header exports are supported via the column mapper.

CSV

CSV export

Comma-separated values with a header row. Common delimiters and BOM encodings are auto-detected.

TXT

Pipe-delimited item master

Positional item-master files (one record per row, pipe-separated) are supported for bulk catalog imports.

Built for the bar JC surveyors set
Compliance-grade infrastructure

RecCheckMD is engineered to clear hospital security review and produce documentation a Joint Commission surveyor can act on without follow-up.

Encrypted file archive

Every uploaded PO persisted in encrypted object storage. Signed, time-limited download links. Defined retention policy.

Tamper-evident audit trail

Every JC compliance state change attributed and timestamped. Every alert links back to the source FDA record. Every action is verifiable.

Hourly FDA monitoring

Background monitor pulls from openFDA every hour with a 14-day safety overlap. New recall hits trigger push notifications within minutes.

Org-scoped access

Auth0-backed login, organization-scoped data, role-aware permissions. No cross-customer data exposure under any condition.

Ready to screen your supply chain?

Upload your file and get a prioritized recall report in under two minutes.

Start Recall Screening

RecCheck Assistant

AI-powered recall & compliance help

Hi! I'm your RecCheckMD Assistant

Ask me anything about your recalls, vendor risk, or compliance status.

Search
Find recalls in seconds

Filter your alerts by vendor, severity, age, or status — I'll surface what matches.

Tip: press ⌘ K (or Ctrl K) to open me from anywhere · type / for commands

The recall assistant is for hospital teams.

RecCheckMD's AI assistant analyzes your purchase orders and FDA recall matches to surface what needs action. Sign in to use it — or request a demo to see it work on real hospital data.