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FDA Introduces Innovative Proposal to Advance Consumer Access to Nonprescription Drugs

Murilo Freitas - 14:12, 26 de junio de 2022323
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FDA Introduces Innovative Proposal to Advance Consumer Access to Nonprescription Drugs
http://www.fda.gov/news-events/press-announcements/fda-introduces-innovative-proposal-advance-consumer-access-nonprescription-drugs

 
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FDA Infant Formula Update: June 27, 2022

Murilo Freitas - 13:14, 26 de junio de 2022291
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FDA Infant Formula Update: June 27, 2022
http://www.fda.gov/news-events/press-announcements/fda-infant-formula-update-june-27-2022

 
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FDA Roundup: June 24, 2022

Murilo Freitas - 19:53, 23 de junio de 2022321
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FDA Roundup: June 24, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-june-24-2022

 
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FDA Releases Action Plan for Rare Neurodegenerative Diseases, Including ALS

Murilo Freitas - 15:37, 22 de junio de 2022345
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FDA Releases Action Plan for Rare Neurodegenerative Diseases, Including ALS
http://www.fda.gov/news-events/press-announcements/fda-releases-action-plan-rare-neurodegenerative-diseases-including-als

 
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FDA Denies Authorization to Market JUUL Products

Murilo Freitas - 14:27, 22 de junio de 2022373
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FDA Denies Authorization to Market JUUL Products
http://www.fda.gov/news-events/press-announcements/fda-denies-authorization-market-juul-products

 
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Baxter Healthcare Corporation Recalls Volara System For Risk Of Respiratory Distress In Ventilated Patients During Home Use

Murilo Freitas - 04:00, 22 de junio de 2022442
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When the Volara system’s in-line ventilator adaptor is used at home with a ventilator, it may prevent the patient from getting enough oxygen.

http://www.fda.gov/medical-devices/medical-device-recalls/baxter-healthcare-corporation-recalls-volara-system-risk-respiratory-distress-ventilated-patients

 
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Medtronic Recalls HeartWare HVAD System Batteries Due to Battery Failure

Murilo Freitas - 04:00, 22 de junio de 2022380
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The welding defect may cause the battery to malfunction and no longer provide power or prevent the battery from holding a full charge or properly recharging.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-heartware-hvad-system-batteries-due-battery-failure

 
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FDA Infant Formula Update: June 22, 2022

Murilo Freitas - 19:30, 21 de junio de 2022336
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FDA Infant Formula Update: June 22, 2022
http://www.fda.gov/news-events/press-announcements/fda-infant-formula-update-june-22-2022

 
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FDA Provides Update on Efforts to Increase Supply and Availability of Safe and Nutritious Infant Formula

Murilo Freitas - 18:35, 21 de junio de 2022357
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FDA Provides Update on Efforts to Increase Supply and Availability of Safe and Nutritious Infant Formula
http://www.fda.gov/news-events/press-announcements/fda-provides-update-efforts-increase-supply-and-availability-safe-and-nutritious-infant-formula

 
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BD Announces Voluntary Recall on Intraosseous Products

Murilo Freitas - 04:00, 21 de junio de 2022363
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BD (Becton, Dickinson and Company), a leading global medical technology company, announced a voluntary recall on the BD Intraosseous Needle Set Kits, BD Intraosseous Manual Driver Kits and BDTM Intraosseous Powered Drivers.

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-announces-voluntary-recall-intraosseous-products

 
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