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# Ambu Recalls its SPUR II Resuscitators
- URL: https://www.fdaweb.com/ambu-recalls-its-spur-ii-resuscitators/
- Published: 2025-08-29T12:00:00.000Z
- Updated: 2026-09-14T15:20:31.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5159787

Ambu is recalling (Class 1) its SPUR II resuscitators due to the manometer port being blocked, which causes the manometer to become non-functional. “This defect can lead to an increased risk of harm caused by pressure changes (barotrauma) and delayed ventilation, since the ventilation pressure applied with Ambu SPUR II cannot be read on the manometer,” a [recall notice](https://links-2.govdelivery.com/CL0/https:%2F%2Fwww.fda.gov%2Fmedical-devices%2Fmedical-device-recalls%2Fmanual-resuscitator-recall-ambu-inc-removes-spur-ii-resuscitators-due-blocked-manometer-port%3Futm%5Fmedium=email%26utm%5Fsource=govdelivery/1/01010198f632f0de-73dc66a2-f764-4339-922c-7597e8ef4f46-000000/XUvh5mmiYGBk2R0FYAoZHsFsInmP4fb3ImNnUysqyxc=420?ref=fdaweb.com) says. “The use of affected product may cause serious adverse health consequences, including barotrauma, collapsed lung (pneumothorax), and death.” To date, there have been no reported injuries associated with this issue.

The Ambu SPUR II resuscitator is a single-patient-use resuscitator intended for pulmonary resuscitation and emergency respiratory support.