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

Recall Z-0529-2022 — Baxter Spectrum IQ Infusion Pumps, Product code 3570009.

U.S. FDA — Device Enforcement · United States · 2021-12-29 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0529-2022
Date of alert
2021-12-29
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00085412610900
Reported risk: There is the potential for reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms when using Spectrum V8 and Spectrum IQ infusion pumps.
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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