Ambu Inc. recalls

3 recalls on record · latest: July 9, 2025

Official U.S. recall history for Ambu Inc., compiled from official government records.

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Ambu Inc. recalls Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult R…

July 9, 2025 · Medical device recalls High risk Potential for the manometer port being blocked rendering the manometer non-func…

Ambu aScope 5 Broncho HD 5 recalled over labeling errors

April 7, 2025 · Medical device recalls Moderate risk Incorrect labeling in which the front red pouch label did not match the actual…

Ambu Inc. recalls Ambu¿ VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr (Ca…

September 16, 2024 · Medical device recalls Moderate risk Ambu has received complaints on Ambu¿ VivaSight 2 DLTs regarding hyper angulati…