Smiths Medical recalled certain sizes of its Portex oral/nasal endotracheal tubes because of a manufacturing defect that results in a smaller diameter, which could potentially lead to inadequate ...
The UK Medicines and Healthcare products Regulatory Agency (MHRA) has introduced new monthly safety bulletins aimed at making ...
Over 16,000 units of Woolite Delicates laundry detergent were voluntarily recalled by the brand after it was discovered that ...
Woolite Delicates laundry detergent units were recalled due to potential bacterial contamination with Pseudomonas. Here’s a list of affected products.
The FDA has labeled Smiths Medical's recall of ProPort Implantable Plastic Port as Class I, the most serious kind.
The business, acquired by ICU Medical in 2022, has been dealing with a series of recalls and quality issues over the past ...
Problematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
Medtronic (MDT) stock turned lower as the FDA announced a most serious type of recall involving its Pipeline Vantage 027 ...
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