All Recalls

95,083 total recalls in our database

SMALL ATTACHMENT, J-LATCH

The Anspach Effort

🏥 Medical Devices Class I - Dangerous

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Oct 6, 2016 Other Medical Devices Nationwide View Details →

Reported customer complaints of automated hematology analyzers catching fire due to misalignment of an internal protective sheet that shields electronic components from salty reagents. Build-up of salt deposits on unprotected electronic components may combust due to heat generated by electronics when instrument cycles. Completed CAPA identified the root cause as supplier providing defective component (sensor ready valve) and the misalignment of the electronic protective shield during manufacturing of the device.

Mar 23, 2017 Other Medical Devices Nationwide View Details →

They may not have been sealed prior to sterilization. Products with unsealed pouches will be non-sterile.

Mar 30, 2017 Other Medical Devices Nationwide View Details →

Methylene Blue, Solution #3 in the Kwik Diff Kit was not Methylene Blue but Crystal Violet instead.

Mar 15, 2017 Other Medical Devices Nationwide View Details →