Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 2,113–2,124 of 2,908 recalls
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.
Identified faulty cartridges. If such a faulty cartridge is used for sample testing, false test results could occur.
The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
The potential for cracks forming in the breathing circuit hose.
The potential for cracks forming in the breathing circuit hose.
The potential for cracks forming in the breathing circuit hose.
The potential for cracks forming in the breathing circuit hose.
The potential for cracks forming in the breathing circuit hose.
The potential for cracks forming in the breathing circuit hose.