Olympus Issues Recall Correction for Bronchoscopes
The US Food and Drug Administration noted that use of devices may cause serious injury or death, but products are not being removed at this time.
Source: medscape.com
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Philips North America LLC Recalls Panorama 1.0T HFO Due to a Risk of Explosion
The FDA has identified this as a Class I recall, the most serious type of recall
Source: itnonline.com
Cordis US Corp Recalls INFINITI Angiographic Catheter due to Products Being Shipped Without Undergoing Sterilization Procedures
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death
Source: dicardiology.com
FDA Warns Against Neptune's Fix Because of Serious Health Risks
The FDA is warning consumers not to use Neptune's Fix or other tianeptine products because of seiorus health risks, including seizures.
Source: foodpoisoningbulletin.com
Fatal Reaction Risks On Certain Seizure Medications: A FDA Warning
FDA alerts on seizure meds' fatal reactions. Stay informed about the risks and safeguard yourself. Read more.
Source: sci-tech-today.com