All Recalls

92,900 total recalls in our database

🏥 Medical Devices Class I - Dangerous

Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing, but that may have been reprocessed, which may lead to devices not performing as intended.

Jul 2, 2024 Other Medical Devices Nationwide View Details →

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

Mar 22, 2024 Implants & Prosthetics Nationwide View Details →

Due to a software issues, after the instrument processes 250 racks cumulatively, any subsequent racks with samples requiring rerun/reflex will be held in the Sample Handler's Buffer area and and error code "9000" will be reported. This issue may cause a delay of results.

Jul 10, 2024 Diagnostic Equipment Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

1)If Complete Blood Count with differential and reticulocyte(CBC+Diff+Retic) sample is run, then immediately following on same rack CBC+Diff sample is run, then falsely low red blood cell count may occur, generating falsely high Mean Cell Hemoglobin(MCH)/MCHC and falsely low hematocrit results. 2)Cell events may be incorrectly counted as basophil(BASO), resulting in increased BASO and %BASO counts

Jun 14, 2024 Other Medical Devices Nationwide View Details →