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

Recall Z-1050-2019 — LW Scientific ZIP IQ Combo Centrifuge, ZIC-CMBO-4RT3 Rev B Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit tubes with additional rotors to spin other fluids in test tubes (15ml and 50ml), microtubes, and PCR strips

U.S. FDA — Device Enforcement · United States · 2019-02-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1050-2019
Date of alert
2019-02-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
LW Scientific, Inc.
Product category
device
Product type
Devices
Reported risk: The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging the surrounding area.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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