All Recalls

95,018 total recalls in our database

CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.

Apr 23, 2024 Prescription Drugs Nationwide View Details →

Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.

Mar 13, 2024 Implants & Prosthetics Nationwide View Details →

Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).

Mar 13, 2024 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

On ultrasound systems, when Cardiac DICOM SR feature is configured to display either minimum or maximum measured value, and multiple cardiac region measurements are made, and results are exported into the SR feature, then The SR viewer will display the LAST measured value, not min or max, which could contribute to patient condition misdiagnosis or negatively influence patient management decisions.

Feb 23, 2024 Diagnostic Equipment Nationwide View Details →

Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles).

Mar 13, 2024 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment

Mar 22, 2024 Other Medical Devices Nationwide View Details →