🏥 Medical Devices Class I - Dangerous
Firm received feedback form the market regarding breakage of the plastic joint which connects the back to the seat.
All Recalls
95,050 total recalls in our database
🏥 Medical Devices Class I - Dangerous
The staplers may have an insufficient firing stroke to break the washer and completely form staples.
🏥 Medical Devices Class I - Dangerous
The staplers may have an insufficient firing stroke to break the washer and completely form staples.
MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Model #6103L-S
Compass Health Brands (Corporate Office)
🏥 Medical Devices Class I - Dangerous
Product design change did not receive proper premarket clearance and lacks a 510 (k)
🏥 Medical Devices Class I - Dangerous
Devices were delivered without the required dry ice.
🏥 Medical Devices Class I - Dangerous
The staplers may have an insufficient firing stroke to break the washer and completely form staples.
In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.
Tissu-Trans FILTRON 100, Catalog 3-TT-FILTRON 100, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Shippert Medical Technologies
🏥 Medical Devices Class I - Dangerous
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.
SureSigns VS3 NBP, SpO2, Product Number 863071. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Philips North America
🏥 Medical Devices Class I - Dangerous
System software inhibits the monitor and as a result does not measure, display and alarm for pulse rates above 240 beats per minute.
Tissu-Trans FILTRON 500, Catalog 3-TT-FILTRON 500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Shippert Medical Technologies
🏥 Medical Devices Class I - Dangerous
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.
🏥 Medical Devices Class I - Dangerous
Devices were delivered without the required dry ice.
In affected Artis systems the movement of the floating tabletop may be blocked after a collision sensor has been activated during system movement.
MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, Model #6104S-S
Compass Health Brands (Corporate Office)
🏥 Medical Devices Class I - Dangerous
Product design change did not receive proper premarket clearance and lacks a 510 (k)
BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with the BD Veritor System Test Devices. Catalog Number: 256066
Becton Dickinson &
🏥 Medical Devices Class I - Dangerous
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
SureSigns VS4 Government Bundle, Product Number 863286. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Philips North America
🏥 Medical Devices Class I - Dangerous
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.
🏥 Medical Devices Class I - Dangerous
Stability did not meet acceptance criteria for visual appearance during mixing and force vs. displacement at 6 months
Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
Moller Vital
🏥 Medical Devices Class I - Dangerous
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.
🏥 Medical Devices Class I - Dangerous
Devices were delivered without the required dry ice.
Tissu-Trans MEGA 1500, Catalog 3-TT-MEGA 1500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Shippert Medical Technologies
🏥 Medical Devices Class I - Dangerous
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.