Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1907-2025 — Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670

U.S. FDA — Device Enforcement · Japan · 2025-04-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1907-2025
Date of alert
2025-04-30
Country / jurisdiction
Japan
Risk level
Class II
Risk type
recall
Brand
Beckman Coulter Mishima K.K.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
14987666540664
Reported risk: A manufacturing defect in the sample probe (S probe). The corners of the tip of the defective S probe are rounded and chamfered, which can prevent the proper formation of the "air layer" required for normal dispensing. The air layer is the air space that separates the cleaning water filled in the probe from the sample sucked into the probe. Maintaining this air space prevents the cleaning water and the sample from mixing. In the defective S probe, the "air layer" was not properly formed, causing the cleaning water and the sample to mix diluting the sample. As a result, the sample mixture dispensed into the cuvette has a lower concentration than the original sample, and the analyte concentration measured is lower than expected results.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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