Blog – Page 27 – PRAIS 2.0

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PAHO and Resolve to Save Lives strengthen partnership to bolster epidemic preparedness across the Americas

admin - 20:34, 24 de July de 2025347

PAHO and Resolve to Save Lives strengthen partnership to bolster epidemic preparedness across the Americas

Cristina Mitchell

25 Jul 2025

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PAHO and Resolve to Save Lives partner for epidemic preparedness in the Americas

admin - 20:34, 24 de July de 2025164

PAHO and Resolve to Save Lives partner for epidemic preparedness in the Americas

Cristina Mitchell

25 Jul 2025

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Disposable Surgical Stapler Cartridge Correction: Ethicon Endo-Surgery, LLC Issues Correction for Endopath Echelon to Address Inadvertent Lockout During Surgical Procedures

Murilo Freitas - 04:00, 24 de July de 2025219

Ethicon Endo-Surgery is correcting the Endopath Echelon due to a potential surgical lockout that stops cutting or stapling and requires extra removal steps.

http://www.fda.gov/medical-devices/medical-device-recalls/disposable-surgical-stapler-cartridge-correction-ethicon-endo-surgery-llc-issues-correction-endopath

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Arterial Cannula Recall: Edwards Lifesciences Removes Arterial Cannula due to Risk of Wire Exposure

Murilo Freitas - 04:00, 23 de July de 2025293

Edwards recalls arterial cannulae due to risk of wire exposure that may cause serious patient harm.

http://www.fda.gov/medical-devices/medical-device-recalls/arterial-cannula-recall-edwards-lifesciences-removes-arterial-cannula-due-risk-wire-exposure

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HHS, FDA and USDA Address the Health Risks of Ultra-Processed Foods

Murilo Freitas - 21:44, 22 de July de 2025251

HHS, FDA and USDA Address the Health Risks of Ultra-Processed Foods
http://www.fda.gov/news-events/press-announcements/hhs-fda-and-usda-address-health-risks-ultra-processed-foods

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Mobile Lift Component Recall: Baxter Healthcare Corporation Removes Mobile Lift Component due to Risk of Improper Attachment

Murilo Freitas - 04:00, 22 de July de 2025331

Baxter is removing mobile lift components due to risk of false attachment, which may result in patient injury due to falls.

http://www.fda.gov/medical-devices/medical-device-recalls/mobile-lift-component-recall-baxter-healthcare-corporation-removes-mobile-lift-component-due-risk

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PAHO Director and CARICOM Secretary-General sign 2025-2029 Joint Subregional cooperation strategy to advance health and equity in the Caribbean

admin - 20:06, 21 de July de 2025201

PAHO Director and CARICOM Secretary-General sign 2025-2029 Joint Subregional cooperation strategy to advance health and equity in the Caribbean

Cristina Mitchell

22 Jul 2025

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HHS, FDA Praise Consumer Brands Association’s Vow to Remove Artificial Colors from America’s Food Supply

Murilo Freitas - 18:17, 21 de July de 2025225

HHS, FDA Praise Consumer Brands Association’s Vow to Remove Artificial Colors from America’s Food Supply
http://www.fda.gov/news-events/press-announcements/hhs-fda-praise-consumer-brands-associations-vow-remove-artificial-colors-americas-food-supply

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Manual Resuscitator Recall: SunMed Holdings, LLC Removes Adult Manual Resuscitator Devices Due to Incorrect Assembly of B/V Filter

Murilo Freitas - 04:00, 21 de July de 2025200

Manual resuscitator recalled due to incorrect B/V filter assembly that could delay therapy. May cause hypoxia, hypercapnia, or death if used.

http://www.fda.gov/medical-devices/medical-device-recalls/manual-resuscitator-recall-sunmed-holdings-llc-removes-adult-manual-resuscitator-devices-due

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Medical Procedure Kits Correction: Medline Industries, LP Issues Correction for Medline Craniotomy Kits Containing Codman Disposable Perforators Due to Risk for Device Disassembly

Murilo Freitas - 04:00, 21 de July de 2025142

Medline Craniotomy Kits are procedure convenience kits. Kits containing the Codman Disposable Perforator are being corrected by Medline Industries.

http://www.fda.gov/medical-devices/medical-device-recalls/medical-procedure-kits-correction-medline-industries-lp-issues-correction-medline-craniotomy-kits