MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, Model #6104S-S
Compass Health Brands (Corporate Office)
Product design change did not receive proper premarket clearance and lacks a 510 (k)
Medical equipment, implants, and diagnostic devices
Compass Health Brands (Corporate Office)
Product design change did not receive proper premarket clearance and lacks a 510 (k)
Becton Dickinson &
Background calibration has the potential to cause false positive or false negative test results. An incorrect test result with the BD Veritor System could lead to possible misdiagnosis and inappropriate treatment
Philips North America
System software inhibits the monitor and as a result does not measure, display and alarm for pulse rates above 240 beats per minute.
The kits may contain the incorrect number of components or the kits may be missing components.
Stability did not meet acceptance criteria for visual appearance during mixing and force vs. displacement at 6 months
Moller Vital
The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall.
Devices were delivered without the required dry ice.
Shippert Medical Technologies
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.
Compass Health Brands (Corporate Office)
Product design change did not receive proper premarket clearance and lacks a 510 (k)
Shippert Medical Technologies
Devices were delivered without the required dry ice.
Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits labeled as containing a 50 cm PICC may contain a 40 cm PICC
Abbott Ireland Diagnostics Division
Patient results may be falsely elevated. This patient impact only applies to patients currently being treated with or recently treated with the drug Mifepristone.
In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.
The staplers may have an insufficient firing stroke to break the washer and completely form staples.
Philips North America
System software inhibits the monitor and as a result does not measure, display and alarm for pulse rates above 240 beats per minute.
Philips North America
System software inhibits the monitor and as a result does not measure, display and alarm for pulse rates above 240 beats per minute.
Shippert Medical Technologies
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.
Philips North America
System software inhibits the monitor and as a result does not measure, display and alarm for pulse rates above 240 beats per minute.
The staplers may have an insufficient firing stroke to break the washer and completely form staples.