company
Covidien LLC
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_recall2026-06-10Covidien LLC — Class II recall: Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
- fda_recall · device_recall2026-06-10Covidien LLC — Class II recall: Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF:…
- fda_recall · device_recall2026-06-10Covidien LLC — Class II recall: Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
- fda_recall · device_recall2026-06-10Covidien LLC — Class II recall: COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI cod…
Frequently asked questions
- How many FDA warning letters has Covidien LLC received?
- Argus HQ has not recorded an FDA warning letter for Covidien LLC in our current dataset.
- What FDA recalls has Covidien LLC issued?
- Argus HQ has recorded 4 FDA recalls tied to Covidien LLC.
- Is Covidien LLC 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 Covidien LLC. 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.