All Recalls

95,018 total recalls in our database

🏥 Medical Devices Class I - Dangerous

When the catheters are used with the EnSiteX EP System, the system does not correctly recognize the catheter as the appropriate product model and instead reads and displays it as a different model. This results in some features specific to the catheter do not appear on the display and the catheter image may also appear inverted.

Dec 18, 2023 Surgical Instruments Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Dec 20, 2023 Other Medical Devices View Details →
🏥 Medical Devices Class I - Dangerous

Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.

Dec 19, 2023 Other Medical Devices View Details →

Due to potential false positive Flu B results when a sample was also SARS-CoV-2 positive.

Dec 15, 2023 Diagnostic Equipment Nationwide View Details →

Achieva 3.0T, Model No. 781177

Philips North America

🏥 Medical Devices Class I - Dangerous

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.

Dec 29, 2023 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.

Dec 29, 2023 Other Medical Devices Nationwide View Details →

Intera 1.5T, Model No. 781195

Philips North America

🏥 Medical Devices Class I - Dangerous

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.

Dec 29, 2023 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

DiaSorin has identified that lots 136344, 136344A, 136344B, 136344C, 136520, 136520A, 136520B, 136520C, 136604, 136703, 136703A, 136703B, 136703C 136775of LIAISON HSV-2 Type Specific IgG assay may produce increased equivocal and/or false positive results.

Dec 13, 2023 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.

Dec 29, 2023 Other Medical Devices Nationwide View Details →

During internal review of Polaris battery assembly data from the HiPot operation, a test systems engineer noticed that some batteries had gone through the High Potential test twice. This was able to occur because the test screen did not prevent retesting after a failure. Some batteries were therefore retested and passed.

Dec 7, 2023 Implants & Prosthetics Nationwide View Details →