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FDA Medical Device Recalls (openFDA)

Beckman Coulter, Inc.: COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conjunction with a cyanide-free lytic agent for counting and sizing blood cells on all UniCel DxH Coulter Cellular Analysis Systems. For use as a rinsing agent on the UniCel DxH Slidemaker Stainers. For use as a diluent in conjunction with DxH ECO Cell Lyse for counting and sizing blood cells. For use as a rinsing agent.

Recall number
Z-1221-2026
Recalling firm
Beckman Coulter, Inc.
Product
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conjunction with a cyanide-free lytic agent for counting and sizing blood cells on all UniCel DxH Coulter Cellular Analysis Systems. For use as a rinsing agent on the UniCel DxH Slidemaker Stainers. For use as a diluent in conjunction with DxH ECO Cell Lyse for counting and sizing blood cells. For use as a rinsing agent.
Status
Open, Classified
Initiated
2025-11-10
Posted
2026-01-30
Terminated
not on file
Reason
Due to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers.
Root cause
Under Investigation by firm
Action
During the week of 11/10/2025, the firm sent via postal and e-mail an "URGENT MEDICAL DEVICE RECALL" Letter to customers informing them that Beckman Coulter has confirmed that specific diluent lot numbers of COULTER DxH Diluent and DxH ECO Diluent may contribute to elevated platelet (PLT) Daily Checks background counts cycle when used with the UniCel DxH 600/690T/800/900 analyzers. Customers are instructed to: "Check their COULTER DxH Diluent and DxH ECO Diluent inventory against the provided affected lot numbers. "If their lot numbers are NOT affected, continue routine operation and no further action is required. "If their lot numbers are affected, perform a Daily Checks cycle. o Each container must be individually verified through Daily Checks before use according to the instructions below. o If Daily Checks pass, continue routine operation and no further action is required, on the active diluent container(s), currently in use. "If the Daily Checks cycle does not pass, follow the instruction provide in the Recall Letter. For questions or further assistance - email BECFA@beckman.com
Quantity
76,098 units (US-61843 and OUS-14255)
Distribution
Worldwide - U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PA, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WV. The countries of Argentina, Canada, Chile, Mexico, Saint Kitts and Nevis, Trinidad and Tobago, and Viet Nam.
Lot, serial or model codes
Catalog Numbers: COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 UDI-DI code: 15099590233686 Lot Numbers: 2510410 2510420 2510450 3557500 3557510 3557540 3557560 3557570 3557640 3557650 3557660 3557670 3557680 3557700 3557710 3557850 3557920 3557930 3558000 3558030 3558040 3558060 3558090 3558100 3558110 3558120 3558140 3558150 3558160 3558170
510(k) numbers
not on file
PMA numbers
not on file
Product code
GIF
Firm FEI
3000203293
Firm city
Miami
Firm state
FL
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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