Murilo Freitas – Página 54

FDA Roundup: November 8, 2022

Murilo Freitas - 23:36, 7 de noviembre de 2022396

FDA Roundup: November 8, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-november-8-2022

FDA Commissioner Tests Positive for COVID-19; Experiencing Mild Symptoms

Murilo Freitas - 23:37, 6 de noviembre de 2022417

FDA Commissioner Tests Positive for COVID-19; Experiencing Mild Symptoms
http://www.fda.gov/news-events/press-announcements/fda-commissioner-tests-positive-covid-19-experiencing-mild-symptoms

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Adam’s Polishes, LLC Issues Voluntary Nationwide Recall of Hand Sanitizer Due to Potential Contamination With Methanol

Murilo Freitas - 05:00, 6 de noviembre de 2022339

Thornton, Colorado, Adam’s Polishes, LLC is voluntarily recalling lot 133475 of Adam’s Polishes Hand Sanitizer to the consumer level. FDA testing has found this lot to contain undeclared methanol. Adam’s Polishes is recalling 19 other lots in an abundance of caution. Persons who accidently ingest (

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/adams-polishes-llc-issues-voluntary-nationwide-recall-hand-sanitizer-due-potential-contamination

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Insulet Issued Voluntary Medical Device Correction for Omnipod DASH® Personal Diabetes Manager on October 17, 2022

Murilo Freitas - 04:00, 4 de noviembre de 2022337

Insulet Corporation (NASDAQ: PODD) (Insulet or the Company), announced on October 17, 2022, a Medical Device Correction for all Omnipod DASH® Personal Diabetes Managers (PDMs) distributed globally. This action was taken voluntarily with the knowledge of the FDA and other regulatory agencies.

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/insulet-issued-voluntary-medical-device-correction-omnipod-dashr-personal-diabetes-manager-october

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FDA Roundup: November 4, 2022

Murilo Freitas - 21:51, 3 de noviembre de 2022429

FDA Roundup: November 4, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-november-4-2022

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Teleflex Announces Worldwide Recall of Gibeck® Iso-Gard® Filter

Murilo Freitas - 04:00, 3 de noviembre de 2022673

Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and surgery, has announced a worldwide recall of affected lots of the below-referenced Gibeck® Iso-Gard® Filter products. The Gibeck® Iso-Gard® Filter is a bacterial and viral filter, intended for

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teleflex-announces-worldwide-recall-gibeckr-iso-gardr-filter

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Do Not Use Infant Head Shaping Pillows to Prevent or Treat Any Medical Condition: FDA Safety Communication

Murilo Freitas - 04:00, 2 de noviembre de 2022543

The FDA recommends that parents, caregivers, and health care providers not to use infant head shaping pillows to prevent or treat any medical condition.

http://www.fda.gov/medical-devices/safety-communications/do-not-use-infant-head-shaping-pillows-prevent-or-treat-any-medical-condition-fda-safety

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