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MicroScan

Beckman Coulter, Inc. · Model B1017-423 · UDI-DI 15099590657987

LRGLQMLTWJWYLTT Prescription
10
510(k) clearances
137
Adverse events (6 deaths)
13
Recalls
10
Facilities

Description

Neg Urine Combo Panel Type 73

Recalls

DateFirmReason
2025-02-12Remel, IncPower supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.
2020-12-02Beckman Coulter Inc.Due to a customer report and internal investigation, it was confirmed that a portion of the affected product lot failed quality control (QC) for ATCC E. Faecalis 29212 versus dapto
2019-10-21Beckman Coulter Inc.WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10
2019-10-21Beckman Coulter Inc.WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10
2019-10-21Beckman Coulter Inc.WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10
2019-10-21Beckman Coulter Inc.WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10
2019-10-21Beckman Coulter Inc.WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10
2019-10-21Beckman Coulter Inc.WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10
2019-09-04Beckman Coulter Inc.Instruments were manufactured with a shortened 30mL reagent draw straw which may result in reagents not dispensing and may lead to organism misidentification and/or Quality Control
2019-09-04Beckman Coulter Inc.Instruments were manufactured with a shortened 30mL reagent draw straw which may result in reagents not dispensing and may lead to organism misidentification and/or Quality Control

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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.