Bausch + Lomb recalls some of its implantable eye lenses
Bausch + Lomb said on Thursday it will recall some of its implantable eye lenses after receiving reports of complications, the cause of which could not immediately be known.
Bausch & Lomb recalls implantable eye lenses due to risk of syndrome that can lead to vision loss
Most cases of TASS can be treated with steroids within a few days, although severe cases can lead to permanent damage to the ...
Dermatology Advisor1d
FDA Testing Reveals Elevated Benzene Levels in Certain OTC Acne Products
A limited amount of retail products containing benzoyl peroxide have been voluntarily recalled after testing for possible benzene contamination.
BDX Stock Declines Following Class I Classification for Alaris Recall
BD's recall of Alaris infusion pumps following software issues has been classified as the most severe recall by the FDA. A suspension of sales may hurt the top line going forward.
Verywell Health2d
Liquid Benadryl Sold on Amazon Recalled Over Risk of Child Poisoning
Bottles of over-the-counter Benadryl sold on Amazon are being recalled nationwide because they pose a safety risk to children ...
News80002d
Trump administration highlights drug cartels as major national security threat but omits climate change
The US intelligence community’s annual threat assessment led with the threat from drug cartels for apparently the first time in the report’s nearly 20-year history, according to Senate ...
Delishably on MSN2d
More Than 10,000 Cans of Coca-Cola are Being Recalled—Here's What You Need to Know
Coca-Cola has issued a recall of over 10,000 cans of its Original Coca-Cola due to the possible presence of foreign material, ...
Over 2,000 Bottles of Benadryl Recalled Due to ‘Child Poisoning’ Risk
Recalls abound, and the latest may be sitting in your medicine cabinet. Over 2,000 bottles of popular allergy medication, ...
American Hospital Association6d
Recall issued for Becton, Dickinson and Company infusion pump adapters
The Food and Drug Administration has identified a Class I recall of Becton, Dickinson and Company BD Alaris Systems Manager and BD Care Coordination Engine Infusion Adapters due to reports that ...
FDA tags Becton, Dickinson and Company infusion software recall as Class I
Problematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
At Least 2,300 Benadryl Bottles Recalled for 'Child Poisoning' Risk
Thousands of bottles of Benadryl, a popular allergy medication, are included in the recall for not having child-resistant ...
Becton Dickinson announces first patient treated in GalaFLEX trial
Becton Dickinson (BDX) announced the first patient treated in an investigational device exemption clinical trial intended to advance BD’s ...