Covidien LLC recalls COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 6088…
Due to customer complaint regarding incorrect display box labeling.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 145–156 of 348 recalls
Due to customer complaint regarding incorrect display box labeling.
Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption…
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product