Covidien, LLC

Frequent Recalls

7

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-03-18 to 2026-08-26

Date	Source	Product	Brand	Severity	Units
2026-08-26	FDA Device	FDA Recall: EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHE	Covidien, LLC	Class II	N/A
2026-07-08	FDA Device	FDA Recall: Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Cod	Covidien LLC	Class II	N/A
2026-06-10	FDA Device	FDA Recall: COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028	Covidien LLC	Class II	N/A
2026-06-10	FDA Device	FDA Recall: Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042	Covidien LLC	Class II	N/A
2026-06-10	FDA Device	FDA Recall: Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044	Covidien LLC	Class II	N/A
2026-06-10	FDA Device	FDA Recall: Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050	Covidien LLC	Class II	N/A
2026-03-18	FDA Device	FDA Recall: HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBAS	Covidien LLC	Class II	N/A