In recent weeks, a drug manufacturer recalled a lot of potassium chloride injections due to a complaint of mislabeling of the overpouch. A medical device manufacturer recalled surgical kits due to a packaging defect that may compromise the sterility of the product. Another device manufacturer recalled a donut gel pillow due to potential mold contamination.
Two medical device manufacturers issued corrections for their products. One manufacturer issued a correction for use of a monitory system, warning that certain medical conditions should not be tested with the system. Another device manufacturer issued a correction for defibrillation electrodes, warning of connector compatibility issues with certain defibrillator units.
View a complete listing of FDA Recalls.
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