95,102 total recalls in our database
Fuchs North America
The product may be potentially positive for Salmonella due to one of the sub-ingredients (oregano) testing positive for Salmonella.
FAILED DISSOLUTION SPECIFICATIONS
The Procter & Gamble Company
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
Superpotent Drug: Out of specification assay result was obtained during stability testing.
Labeling: Missing label: Label missing from some prefilled pens.
FAILED DISSOLUTION SPECIFICATIONS
Presence of particulate matter: particulate identified as a beetle.
Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.
Valor Compounding Pharmacy, Inc
Subpotent and Superpotent Drug
Failed Dissolution Specifications
Jubilant Cadista Pharmaceuticals
Failed Dissolution Specifications
Failed Dissolution Specifications
Jubilant Cadista Pharmaceuticals
Failed dissolution specifications.
GE Healthcare
The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.
Fresenius Medical Care Holdings
Internal ethernet cable may be misaligned, the cable jacket (insulation) could become compromised due to high temperature and result in the internal ethernet cable conducting electrical current to the ethernet port on the outside of the device), potentially harming service technicians and/or other authorized operators. If the ethernet port on the device is touched or manipulated, there is a risk of electrical shock
SIGHT DIAGNOSTICS
The default reference ranges for MCH, MCHC, and RDW for age group "Child 2-11y" are mixed up and incorrectly displayed on OLO devices running software version 2.63, 2.63.1, and 2.63.1.1. Due to the issue, results may incorrectly appear to be within or outside the reference range.
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Manufacturing error that may have resulted in a cathode component being out of specification. All devices met final functional testing requirements.
Kits contain leaking bottles of isopropyl alcohol
Abbott Laboratories
There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
Due to Titanium plasma coating not present implant.