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

Recall Z-1086-2022 — DxM 1096 MicroScan WalkAway Instrument REF B1018-496

U.S. FDA — Device Enforcement · United States · 2019-10-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1086-2022
Date of alert
2019-10-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Beckman Coulter Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
15099590690892
Reported risk: 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 ampere
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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