UniCel DxH800, Part Numbers: 629029 and B24802, automated hematology analyzer
Reported: December 20, 2017 Initiated: November 3, 2017 #Z-0236-2018
Product Description
UniCel DxH800, Part Numbers: 629029 and B24802, automated hematology analyzer
Reason for Recall
The shield for the Single-Tube Station on the DxH instrument may interfere with sample aspiration in the open vial position.
Details
- Recalling Firm
- Beckman Coulter Inc.
- Units Affected
- 15 units
- Distribution
- CA, AR, HI, CA, OH, WA, MD, Canada, Japan
- Location
- Brea, CA
Frequently Asked Questions
What product was recalled? ▼
UniCel DxH800, Part Numbers: 629029 and B24802, automated hematology analyzer. Recalled by Beckman Coulter Inc.. Units affected: 15 units.
Why was this product recalled? ▼
The shield for the Single-Tube Station on the DxH instrument may interfere with sample aspiration in the open vial position.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 20, 2017. Severity: Moderate. Recall number: Z-0236-2018.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11