Every recall we track for Ambu Inc. — 6 in all — plus the complaints and injury reports the public filed about them.
Ambu recalls SPUR II resuscitators with potential manometer port blockage. Check catalog numbers and lot numbers listed to see if your device is affected.
Ambu recalls a specific model of broncho sampler set due to incorrect labeling that could lead to confusion about device size. Affected units have mismatched front and back labels.
Ambu recalls VivaSight 2 DLT endobronchial tubes with hyperangulation risk during intubation. Affected models include 35-41 Fr with specific lot numbers. No remedy provided in recall notice.
Ambu recalls aView 2 monitors with catalog numbers 405011000 and 405011000US2 due to fire risk from using screws longer than 14-16mm. This can cause battery penetration, fire, burns, and smoke inhalation.
Ambu recalls aView 2 Advance monitors made before Oct 29, 2020 that may catch fire if dropped, causing smoke and flames. Affected units have specific model numbers and versions.
Ambu recalls VivaSight 2 DLT endobronchial tube systems due to potential cuff leakage causing airway loss. Affected units have specific catalog numbers and UDI-DI codes. Contact Ambu for remedy.
