rss-es – Página 43 – PRAIS 2.0

FDA Provides Draft Labeling Recommendations for Plant-based Milk Alternatives to Inform Consumers

Murilo Freitas - 15:13, 21 de febrero de 2023246

FDA Provides Draft Labeling Recommendations for Plant-based Milk Alternatives to Inform Consumers
http://www.fda.gov/news-events/press-announcements/fda-provides-draft-labeling-recommendations-plant-based-milk-alternatives-inform-consumers

GE HealthCare Recalls Nuclear Medicine 600/800 Series Systems for Risk of Detector Fall That May Injure Patients

Murilo Freitas - 05:00, 21 de febrero de 2023310

Safety mitigation issues including a failing ball screw and missing safety key may cause the 600/800 Series systems to fall on patients, leading to injury.

http://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

FDA Roundup: February 21, 2023

Murilo Freitas - 21:11, 20 de febrero de 2023281

FDA Roundup: February 21, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-february-21-2023

nanoMaterials Discovery Corporation Issues Voluntary Nationwide Recall of its Alcohol Antiseptic 80% Alcohol Solution

Murilo Freitas - 05:00, 20 de febrero de 2023282

Seattle, Washington, nanoMaterials Discovery Corporation is voluntarily recalling all lots of its Alcohol Antiseptic 80% Alcohol Solution branded as “Snowy Range Blue” in four fluid ounce spray dispenser packaging to the consumer level. Certain batches of the company’s Alcohol Antiseptic 80% Alcoho

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nanomaterials-discovery-corporation-issues-voluntary-nationwide-recall-its-alcohol-antiseptic-80

FDA Roundup: February 17, 2023

Murilo Freitas - 19:50, 16 de febrero de 2023271

FDA Roundup: February 17, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-february-17-2023

Magellan Diagnostics Recalls LeadCare II, LeadCare Plus, and LeadCare Ultra Blood Lead Tests Due to Risk of Falsely Low Results

Murilo Freitas - 05:00, 16 de febrero de 2023469

The LeadCare tests are used to detect blood lead level but has risk of falsely low results.

http://www.fda.gov/medical-devices/medical-device-recalls/magellan-diagnostics-recalls-leadcare-ii-leadcare-plus-and-leadcare-ultra-blood-lead-tests-due-risk

La FDA lleva a cabo actividades adicionales para prevenir las sobredosis de drogas y reducir los fallecimientos

Murilo Freitas - 20:33, 15 de febrero de 2023221

La FDA lleva a cabo actividades adicionales para prevenir las sobredosis de drogas y reducir los fallecimientos
http://www.fda.gov/news-events/press-announcements/la-fda-lleva-cabo-actividades-adicionales-para-prevenir-las-sobredosis-de-drogas-y-reducir-los

FDA Advances Additional Activities to Prevent Drug Overdoses and Reduce Death

Murilo Freitas - 14:58, 15 de febrero de 2023210

FDA Advances Additional Activities to Prevent Drug Overdoses and Reduce Death
http://www.fda.gov/news-events/press-announcements/fda-advances-additional-activities-prevent-drug-overdoses-and-reduce-death

Philips Respironics Recalls Certain Reworked Philips Respironics Trilogy 100/200 and Garbin Ventilators Due to Potential for Silicone Foam Adhesion Failure and Residual PE‐PUR Foam Debris

Murilo Freitas - 05:00, 15 de febrero de 2023468

Certain Philips Respironics Trilogy and Garbin ventilators are recalled due to foam adhesion failure and the risk of residual PE-PUR foam debris.

http://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-reworked-philips-respironics-trilogy-100200-and-garbin

Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PE‐PUR Foam Debris: FDA Safety Communication

Murilo Freitas - 05:00, 15 de febrero de 20231,301

Certain reworked Trilogy ventilators have two recent issues that may cause blockage or debris in the airpath.

http://www.fda.gov/medical-devices/safety-communications/certain-reworked-philips-respironics-trilogy-100200-ventilators-recalled-due-potential-silicone-foam