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Medtronic Recalls StealthStation S8 Application Versions 1.2.0, 1.1.0, 1.0.3, 1.0.2, and 1.0.1 for Software Error that May Cause Incorrect Measurements During Cranial Surgery

Murilo Freitas - 04:00, 4 de June de 2024242
The software error may cause numbers or letters to be missing from the displayed text and may result in the mechanical depth stop being set too short or too long.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-stealthstation-s8-application-versions-120-110-103-102-and-101-software-error-may

 
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HomeoCare Laboratories Inc. Issues Voluntary Nationwide Recall of Homeopathic Stella Life Oral Care Spray Unflavored and Advanced Formula Peppermint Oral Care Rinse Due to Microbial Contamination

Murilo Freitas - 04:00, 4 de June de 2024177
HomeoCare Laboratories Inc., a manufacturer of homeopathic products, is voluntarily recalling two batches of Homeopathic StellaLife Oral Care Products listed in the table below manufactured in 2024 due to FDA findings of microbial contamination. This recall is to be performed at the consumer level.

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/homeocare-laboratories-inc-issues-voluntary-nationwide-recall-homeopathic-stella-life-oral-care

 
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World Health Assembly agreement reached on wide-ranging, decisive package of amendments to improve the International Health Regulations, and sets date for finalizing negotiations on a proposed Pandemic Agreement

admin - 22:15, 31 de May de 2024360
World Health Assembly agreement reached on wide-ranging, decisive package of amendments to improve the International Health Regulations, and sets date for finalizing negotiations on a proposed Pandemic Agreement

Cristina Mitchell

1 Jun 2024

 
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Medline Industries, LP Issues Nationwide Recall of SubG Endotracheal Tube with Subglottic Suction

Murilo Freitas - 04:00, 30 de May de 2024222
On February 20, 2024, Medline Industries, LP initiated a nationwide recall of 6 SubG Endotracheal Tubes with Subglottic Suction and 10 kits that contain these devices. The inflation tube and other device components have become detached and/or torn from the main tube, resulting in moisture buildup, l

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-subg-endotracheal-tube-subglottic-suction

 
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