Maquet Equipment ARDEQT639019ARecalls & reported problems
Maquet Sas · EQTXHS016 SAX14 · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Nov 8, 2023Open, Classified
A potential for a light system to fall in the operating room.
Z-0761-2024 · Root cause: Equipment maintenance · FDA record ↗
Other HOLDER, CAMERA, SURGICAL devices
- Maquet Equipment ARDEQT239016AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239022AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239007AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- NA ARDEQT269002AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239020AMaquet Sas · Holder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDEQT239008AMaquet Sas · Holder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDSAT609000AMaquet Sas · HOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT669005AMaquet Sas · HOLDER, CAMERA, SURGICAL1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.