All Recalls

95,114 total recalls in our database

During internal testing a situation was discovered where when changing the settings, a new setting could not be accepted and potentially result in a discrepancy in the energy delivered (higher or lower) from the value displayed on the Graphical User Interface display.

May 13, 2015 Surgical Instruments View Details →

Possible drug interference when using the Trinder reaction method on multiple Cobas Analyzers. Results of Trinder tests may be falsely decreased when the tests are run with urine samples (Creatinine plus and Uric Acid applications only) or blood samples collected before sufficient time has lapsed after the administration of the drugs Acetaminophen and N-acetylcysteine.

May 7, 2015 Diagnostic Equipment Nationwide View Details →

JustRight Surgical is recalling various lots of JustRight 5mm Stapler product because they may deliver incomplete staple formation and incomplete tissue closure.

Jun 11, 2015 Other Medical Devices Nationwide View Details →

Possible drug interference when using the Trinder reaction method on multiple Cobas Analyzers. Results of Trinder tests may be falsely decreased when the tests are run with urine samples (Creatinine plus and Uric Acid applications only) or blood samples collected before sufficient time has lapsed after the administration of the drugs Acetaminophen and N-acetylcysteine.

May 7, 2015 Diagnostic Equipment Nationwide View Details →

under certain circumstances the Cios Alpha system may freeze during a procedure.

May 5, 2015 Diagnostic Equipment Nationwide View Details →

A firmware bug causes incorrect values to be displayed for specific measured luminescence values.

May 29, 2015 Diagnostic Equipment Nationwide View Details →

GE Healthcare has recently become aware of a potential safety issue that may result in the loss of C-arm gantry motion capability on fluoroscopic Interventional imaging systems (Innova, Optima and Discovery).

May 29, 2015 Diagnostic Equipment Nationwide View Details →

GE Healthcare has recently become aware of a potential safety issue that may result in the loss of C-arm gantry motion capability on fluoroscopic Interventional imaging systems (Innova, Optima and Discovery).

May 29, 2015 Diagnostic Equipment Nationwide View Details →