Covidien, LLC recalls

7 recalls.

• EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 ... recall (Covidien, LLC)
  Medical deviceClass IIReported August 26, 2026 · The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.
• Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 ... recall (Covidien LLC)
  Medical deviceClass IIReported July 8, 2026 · Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.
• Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050 recall (Covidien LLC)
  Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance.
• Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 recall (Covidien LLC)
  Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance.
• Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042 recall (Covidien LLC)
  Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance.
• COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code:... recall (Covidien LLC)
  Medical deviceClass IIReported June 10, 2026 · Due to customer complaint regarding incorrect display box labeling.
• HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product... recall (Covidien LLC)
  Medical deviceClass IIReported March 18, 2026 · Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote...