DxH

Beckman Coulter, Inc. · Model C67251 · UDI-DI 15099590744854

GGK Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

DxH ECO Cell Lyse is a cyanide-free reagent that measures hemoglobin by the oxyhemoglobin method. Surfactants are used to lyse the erythrocytes and release the hemoglobin. The released oxyhemoglobin reacts with an antioxidant and a stabilizing reagent, converting the oxyhemoglobin into a stable hemochromogen, which is photometrically measured by the instrument. The lytic reagent also solubilizes the red blood cell membrane while simultaneously preserving the white blood cell and NRBC cellular morphology to be counted and sized.

Recalls

Date	Firm	Reason
2022-05-25	Mckesson Medical-Surgical Inc. Corporate Office	Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0
2011-07-11	Beckman Coulter Inc.	The recall was initiated because Beckman Coulter identified unexpected high particle counts in the lots of DxH Cell Lyse listed. These lots may generate high background counts; cou
2011-04-11	Sysmex America, Inc.	The affected lots of Stromatolyser-IM lysing reagent were found to be contaminated with Pseudomonas bacteria, which resulted in rising IMI channel background counts, increased fals
2011-04-08	Beckman Coulter Inc.	The recall was initiated because Beckman Coulter has confirmed that an issue has been identified with one of the raw materials used to manufacture the Coulter A T 5 diff PN 8547171
2010-12-28	Beckman Coulter Inc.	The recall was initiated by Beckman Coulter because the COULTER LYSE III diff Lytic Reagent Lot number 101554F was released for distribution to customers between November 17 and De
2009-06-23	Sysmex America, Inc.	The affected lots of Stromatolyser-IM lysing reagent was found to be contaminated with Pseudomonas bacteria, which resulted in rising IMI channel background counts, increased false
2007-12-19	Abbott Laboratories	Microbial Contamination: The WBC (White Blood Cell) Reagent Part A was confirmed positive for Pseudomonas contamination.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.