Labeling Updates for BD Mesh Products - Letter to Health Care Providers
The safety and effectiveness of surgical mesh in breast surgery, including in augmentation and reconstruction of the breast, has not been determined by the FDA.
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The safety and effectiveness of surgical mesh in breast surgery, including in augmentation and reconstruction of the breast, has not been determined by the FDA.
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Dans le traitement de la schizophrénie chez l'adulte.
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The Teleflex and Arrow International, Pressure Injectable Catheter Kits are being recalled for incorrect labeling of the product code and product name.
Nurse Assist, LLC initiated a voluntary recall of 0.9% sodium chloride irrigation USP and sterile water for irrigation USP, due to the potential for a lack of sterility assurance, which could result in a nonsterile product. In populations most at risk, such as patients who are immunocompromised, the
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