All Recalls

95,114 total recalls in our database

πŸ₯ Medical Devices Class I - Dangerous

The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.

Jul 23, 2014 Other Medical Devices Nationwide View Details β†’

Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a component that can cause the device to malfunction.

Jul 10, 2014 Other Medical Devices Nationwide View Details β†’

To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure specification outlined in the product's Instructions for Use (IFU).

Jul 3, 2014 Implants & Prosthetics Nationwide View Details β†’

Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a manufacturing issue that has the potential to compromise the water resistance of the affected Guardian monitors.

Jul 21, 2014 Diagnostic Equipment Nationwide View Details β†’

Some sheets of the medical screen film are fogged.

Jul 16, 2014 Diagnostic Equipment Nationwide View Details β†’

To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure specification outlined in the product's Instructions for Use (IFU).

Jul 3, 2014 Implants & Prosthetics Nationwide View Details β†’

Nanosphere Inc. has recently determined through four customer complaints that a small number of Verigene Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) Extraction Trays in Lot 042914021B have low levels or are missing Magnetic Microparticles (MMPs) required for DNA Extraction.

Jul 9, 2014 Diagnostic Equipment Nationwide View Details β†’
πŸ₯ Medical Devices Class I - Dangerous

Nanosphere has received report of an increased rate of "No Call - INT CTL 2" results for the Internal Control 2 (INT CTL 2) when negative samples are tested with certain lots of CDF Amplification Trays (20-011-022), which are contained in the CDF Amplification Reagent Kit (20-012-022); specifically for lots 061913022D and 071813022E.

Oct 16, 2013 Diagnostic Equipment View Details β†’

To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure specification outlined in the product's Instructions for Use (IFU).

Jul 3, 2014 Implants & Prosthetics Nationwide View Details β†’
πŸ₯ Medical Devices Class I - Dangerous

The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.

Jul 23, 2014 Other Medical Devices Nationwide View Details β†’