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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

37,779 Total Recalls

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 →
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 →

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

Mar 22, 2024 Surgical Instruments Nationwide View Details →

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

Mar 22, 2024 Other Medical Devices Nationwide View Details →