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Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution

Murilo Freitas - 04:00, 11 de marzo de 2024154
Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulate

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-pharmaceutical-issues-voluntary-nationwide-recall-one-lot-treprostinil-injection-due-potential

 
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Windstone Medical Packaging, Inc. Recalls Local Lower Extremity Pack, In House Ocular Pack and Closure Kit Containing Sterile Water Based Products Under Recall by Nurse Assist

Murilo Freitas - 04:00, 10 de marzo de 202492
Windstone Medical Packaging recalls kits (Lower Extremity, Ocular, Closure) due to sterility concerns linked to Nurse Assist’s November 6, 2023, recall.

http://www.fda.gov/medical-devices/medical-device-recalls/windstone-medical-packaging-inc-recalls-local-lower-extremity-pack-house-ocular-pack-and-closure-kit

 
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Abbott Recalls HeartMate Touch Communication System for Unintentional Pump Start and Stop

Murilo Freitas - 04:00, 10 de marzo de 202499
The Abbott HeartMate Touch Communication System is being recalled due to the risk of unintended communication with the HeartMate System Controller resulting in pump stop of the HeartMate 3 Left Ventricular Assist Device.

http://www.fda.gov/medical-devices/medical-device-recalls/abbott-recalls-heartmate-touch-communication-system-unintentional-pump-start-and-stop

 
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Ventec Life Systems Recalls VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) for Manufacturing Issue with Bonded Spiral Wrap

Murilo Freitas - 05:00, 6 de marzo de 202474
If the bonded spiral wrap detaches, it can compromise the structural integrity, functionality, or cause blockage, stoppage, or leaks in the breathing circuit.

http://www.fda.gov/medical-devices/medical-device-recalls/ventec-life-systems-recalls-vocsn-patient-breathing-package-pediatric-active-oxygen-blue

 
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Medtronic Neurosurgery Recalls Duet External Drainage and Monitoring System Catheter Tubing due to a Potential for the Catheter Disconnection from the Patient Line Stopcock Connectors

Murilo Freitas - 05:00, 6 de marzo de 202496
Medtronic Neurosurgery is recalling Duet EDMS catheter tubing due to a potential for disconnection from the patient line stopcock connectors.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-neurosurgery-recalls-duet-external-drainage-and-monitoring-system-catheter-tubing-due

 
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