Maquet EquipmentRecalls & reported problems across all models
Maquet Sas · 45 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Maquet Equipment model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 45 models of Maquet Equipment by Maquet Sas in the FDA's device registry (GUDID). Together they are named in 8 adverse event reports in the FDA's MAUDE database, received between Jun 5, 2023 and Dec 23, 2025 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (6 reports).
1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Maquet Equipment recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 8, 2023Open, Classified
A potential for a light system to fall in the operating room.
Z-0761-2024 · Root cause: Equipment maintenance · names 43 of these models · Recall details · FDA record ↗
Most reported Maquet Equipment problems
Device problems
- Detachment of Device or Device Component6
- Peeled/Delaminated2
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Maquet Equipment models
45 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Maquet Equipment ARDSAT239007AHolder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDEQT239016AHolder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239020AHolder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239022AHolder, Camera, Surgical1 recall1 report
- Maquet Equipment ARDSAT239006AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDSAT239010AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDSAT239013AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239010AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239014AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDSAT239016AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT239018AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239017AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDSAT239018AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDSAT229007AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239020AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239022AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239012AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239008AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239026AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239028AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT239024AHolder, Camera, Surgical1 recall0 reports
- Maquet Equipment ARDEQT639014AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639015AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639025AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT609000AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT669008AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639007AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639009AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639011AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639017AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639019AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639021AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639023AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT639027AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT669002AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT629008AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639005AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639007AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639009AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639013AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639019AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT639021AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDSAT669005AHOLDER, CAMERA, SURGICAL1 recall0 reports
- Maquet Equipment ARDEQT239015AHOLDER, CAMERA, SURGICAL2 reports
- Maquet Equipment ARDSAT239019AHolder, Camera, Surgical2 reports
Recent Maquet Equipment adverse event reports
The 8 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionDec 23, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23876021 ↗MalfunctionJan 30, 2025Peeled/Delaminated; Peeled/Delaminated
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR SURGICAL EQUIPMENT - EQTXS3216. IT WAS STATED THE PAINT WAS BUBBLING/CHIPPING ON THE SPRING ARM. WE DECIDED TO REPORT THE ISSUE IN ABUNDANCE OF CAUTION AS ANY PAINT PARTICLES FALLING OFF INTO STERILE FIELD OR DURING PROCEDURE MAY CAUSE CONTAMINATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21273222 ↗MalfunctionJan 30, 2025Peeled/Delaminated; Peeled/Delaminated
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21273092 ↗MalfunctionJan 9, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21109461 ↗MalfunctionAug 22, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
ON 31ST JULY, 2024 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF EQUIPMENT - XHSO. IT WAS STATED THE HANDLE FELL OFF FROM SCREEN HOLDER DURING OPERATION. WE DECIDED TO REPORT THE ISSUE IN ABUNDANCE OF CAUTION AS ANY PARTS FALLING OFF INTO STERILE FIELD OR DURING PROCEDURE MAY CAUSE CONTAMINATION OR SERIOUS INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20037486 ↗MalfunctionOct 19, 2023Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
ON (B)(6), 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF SURGICAL EQUIPMENT - S/E BRAS SIMPLE SALMS. IT WAS STATED THE MONITOR ARM HAD BROKEN AND MONITOR HAD BECOME DETACHED. PHOTOGRAPHIC EVIDENCE CONFIRMED THAT ISSUE AND ALSO INDICATED THAT PAINT WAS DAMAGED ON MONITOR ARM. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE IN ABUNDANCE OF CAUTION AS ANY PARTS OR PARTICLES FALLING OFF INTO STERILE FIELD OR DURING PROCEDURE MAY CAUSE CONTAMINATION OR SERIOUS INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17963615 ↗MalfunctionSep 19, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
ON (B)(6) 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF SURGICAL LIGHTS - VOLISTA ACCESS. IT WAS STATED THE FIXING BASE FOR THE MONITOR FROM THE MONITOR HOLDER WAS MISSING. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE IN ABUNDANCE OF CAUTION AS ANY PARTS FALLING OFF INTO STERILE FIELD OR DURING PROCEDURE MAY CAUSE CONTAMINATION OR SERIOUS INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17771907 ↗MalfunctionJun 5, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
ON 29TH MAY, 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF SURGICAL EQUIPMENT ¿ EQTXHS021 SAT12. IT WAS STATED THE HANDLE HAS COME OFF FROM THE MONITOR HOLDER DURING SURGERY. IT WAS CONFIRMED THERE WAS NO HARM TO A PATIENT'S HEALTH. WE DECIDED TO REPORT THE ISSUE IN ABUNDANCE OF CAUTION AS ANY PARTS FALLING OFF INTO STERILE FIELD OR DURING PROCEDURE MAY CAUSE CONTAMINATION OR SERIOUS INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17066633 ↗
Other Maquet Sas products
- Maquet PowerLED II992 models · 138 reports · 1 recall
- POWERLED TM280 models · 79 reports · 2 recalls
- STANDOP VOLISTA23 models · 56 reports · 1 recall
- Maquet Rolite17 models · 1 reports · 2 recalls
- LUCEA LED33 models · 51 reports · 1 recall
- ROLITE VOLISTA STANDOP8 models · 0 reports · 2 recalls
- Maquet Orchide5 models · 4 reports · 1 recall
- POWERLED2 models · 3 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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