Murilo Freitas – Página 2 – PRAIS 2.0

Recall of Certain Saline and Sterile Water Medical Products Associated with Nurse Assist: FDA Safety Communication

Murilo Freitas - 04:00, 14 de abril de 20241,448

Nurse Assist, LLC announced a recall because the products may not be sterile. Patients are at risk of infection.

http://www.fda.gov/medical-devices/safety-communications/recall-certain-saline-and-sterile-water-medical-products-associated-nurse-assist-fda-safety

2023 Safety Communications

Murilo Freitas - 04:00, 25 de marzo de 20241,128

Listing of Medical Device 2023 Safety Communications

http://www.fda.gov/medical-devices/safety-communications/2023-safety-communications

Evaluating Plastic Syringes Made in China for Potential Device Failures: FDA Safety Communication

Murilo Freitas - 04:00, 18 de marzo de 2024890

Consider using plastic syringes not manufactured in China, if possible.

http://www.fda.gov/medical-devices/safety-communications/evaluating-plastic-syringes-made-china-potential-device-failures-fda-safety-communication

FDA Roundup: March 15, 2024

Murilo Freitas - 20:47, 14 de marzo de 2024495

FDA Roundup: March 15, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-march-15-2024

FDA Approves First Treatment for Patients with Liver Scarring Due to Fatty Liver Disease

Murilo Freitas - 19:58, 13 de marzo de 2024503

FDA Approves First Treatment for Patients with Liver Scarring Due to Fatty Liver Disease
http://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-patients-liver-scarring-due-fatty-liver-disease

Avanos Recalls MIC Gastric – Jejunal Feeding Tube Kits Containing Sterile Water Based Products Under Recall by Nurse Assist

Murilo Freitas - 04:00, 13 de marzo de 2024391

Avanos Recalls Kits Containing Nurse Assist Saline

http://www.fda.gov/medical-devices/medical-device-recalls/avanos-recalls-mic-gastric-jejunal-feeding-tube-kits-containing-sterile-water-based-products-under

FDA Roundup: March 12, 2024

Murilo Freitas - 19:54, 11 de marzo de 2024375

FDA Roundup: March 12, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-march-12-2024

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 2024348

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

FDA Seeks $7.2 Billion to Enhance Food Safety and Nutrition, Advance Medical Product Safety, and Strengthen Public Health

Murilo Freitas - 19:01, 10 de marzo de 2024321

FDA Seeks $7.2 Billion to Enhance Food Safety and Nutrition, Advance Medical Product Safety, and Strengthen Public Health
http://www.fda.gov/news-events/press-announcements/fda-seeks-72-billion-enhance-food-safety-and-nutrition-advance-medical-product-safety-and-strengthen

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 2024306

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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