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FDA Encourages the Public to Follow Established Choking Rescue Protocols: FDA Safety Communication

Murilo Freitas - 04:00, 25 de April de 2024261

These choking rescue protocols include abdominal thrusts (also called the “Heimlich” maneuver) for children and adults but not anti-choking devices.

http://www.fda.gov/medical-devices/safety-communications/fda-encourages-public-follow-established-choking-rescue-protocols-fda-safety-communication

Elekta Instrument AB Recalls Disposable Biopsy Needle Kit for Leksell Stereotactic System for Possibly Containing Microscopic Stainless Steel Debris on the Inside of the Biopsy Needle

Murilo Freitas - 04:00, 25 de April de 2024144

Elekta recalls Disposable Biopsy Needles (911933) from batch 837838839 due to potential microscopic stainless steel debris inside.

http://www.fda.gov/medical-devices/medical-device-recalls/elekta-instrument-ab-recalls-disposable-biopsy-needle-kit-leksell-stereotactic-system-possibly

IDB and PAHO Join Forces to Drive Digital Health and Pandemic Preparedness in Latin America and the Caribbean

admin - 18:27, 24 de April de 2024207

IDB and PAHO Join Forces to Drive Digital Health and Pandemic Preparedness in Latin America and the Caribbean

Oscar Reyes

25 Apr 2024

World Malaria Day – PAHO urges countries to step up access to diagnosis and treatment for vulnerable populations

admin - 14:26, 24 de April de 2024207

World Malaria Day – PAHO urges countries to step up access to diagnosis and treatment for vulnerable populations

Oscar Reyes

25 Apr 2024

Outset Medical, Inc. Recalls Certain Tablo Hemodialysis Systems for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBAs

Murilo Freitas - 04:00, 24 de April de 2024218

The Tablo Hemodialysis System may expose patients to higher than allowable levels of NDL-PCBAs.

http://www.fda.gov/medical-devices/medical-device-recalls/outset-medical-inc-recalls-certain-tablo-hemodialysis-systems-risk-patient-exposure-higher-allowable

InfuTronix, LLC Recalls Nimbus and Nimbus II Infusion Pump Systems for Multiple Device Failures That May Cause Severe Injury and Death

Murilo Freitas - 04:00, 24 de April de 2024168

Nimbus and Nimbus II infusion pumps may experience one or more issues that can cause severe patient injury and death.

http://www.fda.gov/medical-devices/medical-device-recalls/infutronix-llc-recalls-nimbus-and-nimbus-ii-infusion-pump-systems-multiple-device-failures-may-cause

FDA Approves New Treatment for Uncomplicated Urinary Tract Infections

Murilo Freitas - 17:32, 23 de April de 2024195

FDA Approves New Treatment for Uncomplicated Urinary Tract Infections
http://www.fda.gov/news-events/press-announcements/fda-approves-new-treatment-uncomplicated-urinary-tract-infections

DeRoyal Industries, Inc. Recalls Tracecarts Containing 16FR Urine Meter Foley Under Recall by Nurse Assist

Murilo Freitas - 04:00, 23 de April de 2024215

DeRoyal is recalling Surgical Tracecarts with Nurse Assist 16FR Silver Urine Meter Foley due to sterility concerns. Other items in the tracecart are unaffected.

http://www.fda.gov/medical-devices/medical-device-recalls/deroyal-industries-inc-recalls-tracecarts-containing-16fr-urine-meter-foley-under-recall-nurse

FDA Roundup: April 23, 2024

Murilo Freitas - 19:20, 22 de April de 2024246

FDA Roundup: April 23, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-april-23-2024

STOP CLOPEZ CORP Issues Voluntary Worldwide Recall of Schwinnng Capsules Due to the Presence of Undeclared Nortadalafil

Murilo Freitas - 04:00, 22 de April de 2024278

Hollywood, FL, US, STOP CLOPEZ CORP is voluntarily recalling one lot of Schwinnng capsules to the consumer level. FDA analysis has found the Schwinnng products to contain Nortadalafil. Nortadalafil is an active drug ingredient known for the treatment of male erectile dysfunction. The presence of Nor

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/stop-clopez-corp-issues-voluntary-worldwide-recall-schwinnng-capsules-due-presence-undeclared

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