95,083 total recalls in our database
Arrow International
Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the affected product due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.
Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may exhibit excessive background noise that may mask the users ability to clearly hear heart rate and/or blood flow.
The firm discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.
The firm identified a negative shift of 5mmol/L for sodium recovery in Synchron Control Level 3 when calibrated with AQUA Cal 1.
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.
bioMerieux
Complaints were received from customers observing falsely overestimate results or external quality control higher results than expected when performing tests with VIDAS Testosterone.
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the malfunctioning device was reported to be twice that of the rate noted on the label.
Pentax initiated a field correction/safety alert for two (2) models of the Video Duodenoscope to determine how soiling may have occurred on the surface of the suction cylinder and under the distal cap during testing.
Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.
Fujifilm Medical Systems U.S.A.
Fujifilm is recalling multiple endoscopes after a retrospective review.
Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may exhibit excessive background noise that may mask the users ability to clearly hear heart rate and/or blood flow.
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.
For lack of evidence to validate effectiveness of sterilization dose, O-Two Medical Technologies Inc. hereby announces a voluntary medical device recall of the suspected batches of Burn Relief¿ products to prevent potential contamination. .
Toshiba American Medical Systems
When Continuous Trace method is used as the tracing method on Spectral Doppler in velocity trace measurement, an incorrect value may be displayed in the ultrasound systems and in the ultrasound workstations listed below.
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.