Categories

Suntegrity Skincare Issues Voluntary Recall of Suntegrity Impeccable Skin Sunscreen Foundation (Multiple Shades) Due to Microbial Contamination

Las Vegas, Nevada. On May 24, 2024, Suntegrity Skincare initiated a voluntarily recall of nine lots of Suntegrity Impeccable Skin Sunscreen Foundation (Multiple Shades) based on its discovery of a higher than acceptable microbiological mold count (Species: Aspergillus Sydowii) in some tubes of Lot 1

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/suntegrity-skincare-issues-voluntary-recall-suntegrity-impeccable-skin-sunscreen-foundation-multiple

 
Categories

Endotracheal Tube Recall: Medline Industries, LP Removes Medline Sub-G Endotracheal Tube with Subglottic Suctioning due to Detachment or Tearing of the Inflation Tube from the Main Tube

Medline Industries, LP is recalling the Sub-G Endotracheal Tube with Subglottic Suction due to detachment or tearing of the inflation tube and other components from the main tube.

http://www.fda.gov/medical-devices/medical-device-recalls/endotracheal-tube-recall-medline-industries-lp-removes-medline-sub-g-endotracheal-tube-subglottic

 
Categories

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

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