Blog – Page 39 – PRAIS 2.0

Monoject U-100 1 ml Insulin Syringe Luer-Lock with Tip Cap Soft Pack is used for IV insulin. Certain lots are incompatible with needleless connectors.

http://www.fda.gov/medical-devices/medical-device-recalls/syringe-recall-cardinal-health-removes-certain-monoject-u-100-ml-insulin-syringe-luer-lock-tip-cap

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FDA Roundup: December 3, 2024

Murilo Freitas - 20:52, 2 de December de 2024205

FDA Roundup: December 3, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-december-3-2024

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USDA-FDA Seek Information About Food Date Labeling, Aim is to Provide Further Clarity, Transparency and Cost Savings for U.S. Consumers

Murilo Freitas - 18:08, 2 de December de 2024200

USDA-FDA Seek Information About Food Date Labeling, Aim is to Provide Further Clarity, Transparency and Cost Savings for U.S. Consumers
http://www.fda.gov/news-events/press-announcements/usda-fda-seek-information-about-food-date-labeling-aim-provide-further-clarity-transparency-and-cost

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El Salvador joins the Alliance for Primary Health Care in the Americas

admin - 21:32, 1 de December de 2024305

El Salvador joins the Alliance for Primary Health Care in the Americas

Cristina Mitchell

2 Dec 2024

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Hemodialysis Correction: Baxter Issues Correction for AK 98 Hemodialysis Machines Due to Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA and/or NDL-PCBs

Murilo Freitas - 05:00, 28 de November de 2024206

Use of Baxter AK 98 hemodialysis machines with less than 500 hours of run time may expose patients to higher than allowable NDL-PCBAs.

http://www.fda.gov/medical-devices/medical-device-recalls/hemodialysis-correction-baxter-issues-correction-ak-98-hemodialysis-machines-due-risk-patient

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Insertion Tube Recall: FHC Removes microTargeting Insertion Tube Sets due to a Manufacturing Size Error That May Lead to Patient Harm

Murilo Freitas - 05:00, 28 de November de 2024209

FHC microTargeting Insertion Tube Sets guide instruments during neurosurgery. The reducing cannula in a specific lot is 20mm too long.

http://www.fda.gov/medical-devices/medical-device-recalls/insertion-tube-recall-fhc-removes-microtargeting-insertion-tube-sets-due-manufacturing-size-error