Class IOngoingZ-2181-2025
Ambu Inc. recalls Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator
Potential for the manometer port being blocked rendering the manometer non-functional.
Ambu Inc.MDAug 20, 2025
Ambu Inc. recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–2 of 2 recalls
Class IIOngoingZ-1723-2025
Ambu Inc. recalls Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product ins…
Ambu Inc.MDMay 14, 2025