company
Merit Medical Systems, Inc.
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-24Merit Medical Systems, Inc. — Class II recall: Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 0088445052…
- fda_recall · device_recall2026-05-06Merit Medical Systems, Inc. — Class II recall: Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
- fda_recall · device_recall2026-05-06Merit Medical Systems, Inc. — Class II recall: Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
- fda_recall · device_recall2026-05-06Merit Medical Systems, Inc. — Class II recall: Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY
Frequently asked questions
- How many FDA warning letters has Merit Medical Systems, Inc. received?
- Argus HQ has not recorded an FDA warning letter for Merit Medical Systems, Inc. in our current dataset.
- What FDA recalls has Merit Medical Systems, Inc. issued?
- Argus HQ has recorded 4 FDA recalls tied to Merit Medical Systems, Inc..
- Is Merit Medical Systems, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 4 recalls, and 0 approval records for Merit Medical Systems, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.