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FDA issues most serious recall for certain speed control dials used for wheelchairs

The Food and Drug Administration has identified a Class I recall of Max Mobility/Permobil SpeedControl Dials used with the SmartDrive MX2+ Power Assist Device for wheelchairs after identifying a design issue that can lead to unexpected behavior of the SmartDrive motor.
Recall Management

Infant formula recall expands as botulism outbreak cases grow

ByHeart Nov. 13 expanded its voluntary recall to include all Whole Nutrition Infant Formula cans and Anywhere Pack products amid an investigation by the Food and Drug Administration and other agencies of a multistate outbreak of infant botulism illnesses.
Recall Management, Quality & Patient Safety

Recall issued for mislabeled potassium chloride

The Food and Drug Administration yesterday published an
COVID-19: CDC, FDA and CMS Guidance, Recall Management

Olympus recalls endoscope needles

The Food and Drug Administration yesterday
Recall Management, COVID-19: CDC, FDA and CMS Guidance

FDA issues most serious recall for certain ventilators 

The Food and Drug Administration has identified a Class I recall of Philips Respironics V30, A30 and A40 ventilators due to the potential for serious injury or death.
Recall Management

FDA issues most serious recall for Edwards Lifesciences cannulas

The Food and Drug Administration has identified a Class I recall of Edwards Lifesciences OptiSite Arterial Perfusion Cannula devices due to the potential for serious injury or death.
Recall Management

Recall issued by FDA for certain craniotomy kits

The Food and Drug Administration has identified a Class I recall of certain lots of Medline Industries Craniotomy Kits containing recalled Codman Disposable Perforators 14mm due to the potential of serious injury or death.
Recall Management, Medical Device Safety

FDA recalls two products for potential of serious harm 

The Food and Drug Administration July 21 identified Class I recalls of two products due to the potential for serious injury of death.
Recall Management

FDA announces recall of cefazolin by Sandoz for mislabeling

The Food and Drug Administration July 15
COVID-19: CDC, FDA and CMS Guidance, Recall Management

FDA issues recall on tubes used to manage bleeding

The Food and Drug Administration has identified a
Recall Management