All Recalls

95,083 total recalls in our database

An increase in claims related to leakage of cerebrospinal fluid (CSF) from the proximal end of the catheter. In the event of a leak going undetected during implantation, it could pose an infectious risk to the patient. The cause of the leaks is indicated to be manufacturing error involving perforation of the inner channel of the catheter during stylet insertion.

Apr 9, 2024 Diagnostic Equipment Nationwide View Details →

Potential for unsealed sterile packing.

Mar 19, 2024 Surgical Instruments View Details →

Issue related to Novalung sensor box, which is a component of the Novalung Console (Part Number F30000163). In certain instances, error messages #206 (yellow) and #208 (red) technical failure, flow measurement during use of the Novalung system.

Apr 8, 2024 Other Medical Devices Nationwide View Details →

Potential for unsealed sterile packing.

Mar 19, 2024 Diagnostic Equipment View Details →
🏥 Medical Devices Class I - Dangerous

Automated external defibrillators have a manufacturing issue that could prevent the device from delivering instructional voice prompts to the user during use of the device. Visual instructional icons will still be present, but this issue could potentially lead to no therapy or a delay in therapy.

Apr 8, 2024 Other Medical Devices Nationwide View Details →