Haemonetics Corporation Recalls

Overview of recall records associated with Haemonetics Corporation, including dates, categories and classifications where available.

2recall records

Jul 6, 2022latest record date

Jul 6, 2022earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceJul 6, 2022

Haemonetics TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034 recall — FDA Z-1310-2022

Due to a shift in the citrated blood reference range for a normal population, the ranges stated in the IFU are changing. If the clinician relies solely on affected results in comparison to…

Class IIFDA: TerminatedHaemonetics Corporation

Medical DeviceJul 6, 2022

Haemonetics TEG5000 Analyzer (07-022, 07-033) with TEG Analytical Software (07-030, 07-031) recall — FDA Z-1298-2022

When the TEG 5000 Analyzer including TEG Analytical Software is used with PlateletMapping (ADP or AA) Assays and TEG Mangement Software, incorrect values of the PlateletMapping ADP or AA %…

Class IIFDA: TerminatedHaemonetics Corporation

Understanding this recall history

This page summarizes recall records in which the official source identifies Haemonetics Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.