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

Recall Z-1497-2019 — Alinity i Processing Module, 03R65 01, with the below components. a. TED (Thermo Electric Device) Engine, Reagent cooler; b. CABLE, POWER OUT, TED CNTRLER Product Usage: The Alinity i processing module is a fully automated immunoassay analyzer allowing random and continuous access, as w

U.S. FDA — Device Enforcement · Germany · 2019-04-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1497-2019
Date of alert
2019-04-05
Country / jurisdiction
Germany
Risk level
Class II
Risk type
recall
Brand
Abbott Gmbh & Co. KG
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
30103732
Reported risk: Potential loose cable connections on the reagent cooler, which could result in temperature errors and eventual reagent cooler failure. Could cause burn and shock injuries to users and a delay in test results. Device design has mitigated this risk, but it is a possibility.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.