95,114 total recalls in our database
Bayer Healthcare Pharmaceuticals
Chemical Contamination: presence of benzene
Bayer Healthcare Pharmaceuticals
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations: LOTRIMIN AF (Tolnaftate 1%) manufactured at the same facility where other lots were found to be contaminated with benzene.
Amneal Pharmaceuticals of New York
Subpotent Drug: Out-of-specification assay result was obtained for Fluocinolone Acetonide.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer Healthcare Pharmaceuticals
Chemical Contamination: presence of benzene
Labelling: Incorrect Exp. Date
Bayer Healthcare Pharmaceuticals
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer Healthcare Pharmaceuticals
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Teva Pharmaceuticals USA
Failed Impurities/Degradation Specifications
Bayer Healthcare Pharmaceuticals
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Bayer Healthcare Pharmaceuticals
Chemical Contamination: presence of benzene
Amneal Pharmaceuticals of New York
Subpotent Drug: Out-of-specification assay result was obtained for Fluocinolone Acetonide.
Due to two issues: 1) Customer complaints associated with greater than expected Rapid Plasma Reagin (RPR) reactivity which does not confirm with treponemal antibody test which may be due to a positive correlation between the mass COVID vaccinations and false reactive RPR results, and 2) During routine stability monitoring, an increase in mean bias above specification was observed which can cause elevated RPR reactivity potentially due to early shelf-life failure.
There is a potential for distal tip dislodgement or separation.
Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and complete the case.
ROi CPS
Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of Specifications was used as a component in some of the ROI CPS, LLC products.
ROi CPS
Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of Specifications was used as a component in some of the ROI CPS, LLC products.
Due to a component in kit being labeled with the incorrect Expiration Date