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RecallsAboutBlog

Covidien LLC

Covidien LLC: 5 recalls listed since March 2026 across FDA.

By year

  • 20265

By agency

  • FDA5

By category

  • Medical Device5

All recalls (5)

EndoFLIP System

The EndoFLIP System can incorrectly flag catheters as expired, making them unavailable for clinical procedures.

Moderate risk, FDA, , Device defect

Covidien Shiley Disposable Decannulation Plug

The Covidien Shiley Disposable Decannulation Plug has incorrect labeling that includes a symbol for non-DEHP, but the product contains DEHP.

Moderate risk, FDA, , Labeling error

Covidien Mon-a-Therm Temperature Probes and Esophageal Stethoscope

Covidien Mon-a-Therm temperature probes lack FDA clearance.

Moderate risk, FDA, , Unapproved product

COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula

The Shiley Tracheostomy Tube has incorrect display box labeling.

Moderate risk, FDA, , Labeling error

HealthCast "Vital Sync" Remote Patient Monitoring System

Alarms from the primary patient bedside monitor may not be transmitted or received on the remote system.

Moderate risk, FDA, , Device defect
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