Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
Implants & Prosthetics
π₯ Medical Devices β’ 4,589 recalls
Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
The device can deliver an atypical amount of energy due to memory corruption inside the device.
Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
The device can deliver an atypical amount of energy due to memory corruption inside the device.
The Truliant Tibial Trial Handle's pin may disassociate from the main body.
Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
The firm received several customer complaints reporting some perioperative breakages of NE0411 Non-Locking screws when inserting the screw into the radius diaphysis
Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x 22mm x 120cm received an ADVANTA v12 7 mm x 38 mm x 80 cm, due to the manifold (catheter hub) was printed as 7mm x 38 mm x 80 cm. The complaint was the result of incorrect dimensional information (7mm x 38mm x 80cm) printed on the manifiold (catheter hub). The complaint device physical dimensions matched the dimensional information displayed on the outer packaging and the device inner pouch. This was the only complaint received for this non-conformance.
Flowonix Medical received a report of a patient implanted with the Prometra II Programmable Pump who may have received a fatal drug overdose during an MRI procedure. The Prometra II pump has an FDA-approved design feature intended to permit safe exposure to an MRI without removing drug from the reservoir.
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 discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.
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 discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.
Incorrect product label. The type of Sewing Ring was mislabeled as being a Standard Sewing Ring instead of an Anatomic Sewing Ring.
The firm discovered a risk of loss of Neuromodulation therapy due to exposure of the IPG to monopolar electrosurgical devices (ESU) during medical procedures.