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

Recall Z-2762-2017 — Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI 00845275000863, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company LLC ,a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA --- For determination of Fib

U.S. FDA — Device Enforcement · United States · 2017-05-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2762-2017
Date of alert
2017-05-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Fisher Diagnostics
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00845275000863
Reported risk: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation Products (FDP) kit, list number 100650, lot 948546 and FDP Latex Reagent, list 100651, lot 890199. While the kit performs accurately at FDP concentrations greater than 20 ¿g/ml, there is an observed reduction in sensitivity when FDP levels are less than 20 ¿g/ml. This reduction in sensitivity has been tied to FDP Latex Reagent lot 890199 and may result in false negatives.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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