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

Recall Z-0032-2022 — Access hsTnI High Sensitivity Troponin I, REF B52699 Access Immunoassay System REAGENT PACK

U.S. FDA — Device Enforcement · United States · 2021-08-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0032-2022
Date of alert
2021-08-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Beckman Coulter Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
15099590693183
Reported risk: Through customer feedback, testing a sample with cardiac troponin I concentration that are >270,000 pg/mL may cause carryover into the hsTnl reagent pack. The carryover is caused by sample-to-pack carryover predominantly into the particle well of the reagent pack by way of the probe. The particle well then becomes contaminated by the high sample from the probe. The extent of the carryover is dependent on sample concentration and frequency of high concentration samples.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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