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

Recall Z-2181-2025 — Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercury Filter, Adult, Catalog Number: 523611051 3 SPUR II Adult Resuscitator, Single Patient Use Resuscitator, Adult, Catalog Number: 523611057 4 SPUR II Adult Resusc

U.S. FDA — Device Enforcement · United States · 2025-07-09 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2181-2025
Date of alert
2025-07-09
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Ambu Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
523211000
Reported risk: Potential for the manometer port being blocked rendering the manometer non-functional.
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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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.