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

Recall Z-2052-2026 — Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software Version: N/A Product Description: The Command Module (91496) is the core of the Spacelabs patient monitoring system, providing the processing power for all basic physiologic par

U.S. FDA — Device Enforcement · United States · 2026-03-26 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2052-2026
Date of alert: 2026-03-26
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Spacelabs Healthcare, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10841522106422

Reported risk: Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester).

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.

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.

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