On Aug. 29, the FDA posted 233 Class I recalls for devices manufactured by Puerto Rico-based Customed on its website, according to the report. Every device was recalled due to errors in packaging.
A Customed news release indicated “the products have been found to have a potential defect due to adhesion. The defect could result in laws of product sterility and lead to infection.”
There have been no reports of serious injuries or deaths reported to the FDA yet, according to the report.
More articles on recalls:
Pharma recalls steady, but increasing in complexity
Drug recalls could hit record high in 2014
7 drug recalls in 2014
Becker’s 3rd Annual Fall Chief Pharmacy Officer Summit is the top tier event that the people leading the future of pharmacy convene. This 3-day event is built specifically for Chief Pharmacy Officers and senior pharmacy leaders. The sessions examine the workforce, financial and clinical priorities shaping pharmacy today. Becker’s is where candid discussions flourish and new ideas thrive. Becker's 3rd Annual Fall Chief Pharmacy Officer Summit
