Haemonetics Corporation: Medical Device Recalls in 2022

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Haemonetics Corporation in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034
Product Name: TEG5000 Analyzer (07-022, 07-033) with TEG Analytical Software (07-030, 07-031) and TEG Platelet Mapping Assay - PlateletMapping ADP & AA (07-014), PlateletMapping ADP (07-015), PlateletMapping AA (07-016). Issue occurs when Platelet Mapping Assay results from a TEG 5000 analyzer are viewed using TEG Manager Software (versions 1.1-4.3.1)