95,083 total recalls in our database
Dr. Reddy's Laboratories
Presence of foreign substance.
Trigen Laboratories
Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications.
CGMP deviations
CGMP deviations
Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.
CGMP Deviations: Out of Specification for Total Aerobic Microbial Count (TAMC) test for unfiltered bulk for decitabine for injection.
CGMP Deviations and Presence of Particulate Matter: Glass
CGMP deviations
CGMP deviations
CGMP deviations
Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Dr. Reddy's Laboratories
Failed Impurities/Degradation Specifications: Related Substances
Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
CGMP deviations
Siemens AG/Siemens Healthcare GmbH
A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Siemens AG/Siemens Healthcare GmbH
A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.
Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical standards when used as a system with automated dispensing cabinet devices, so use may expose user to leakage currents that could cause varying degrees of harm from a minor shock to permanent impairment.
To limit the use of the Mega Soft Pads to patients aged 12 or older to mitigate the potential risk of patient burns identified with use of Mega Soft pads.
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.