Transducer X7-2t 989605461941Recalls & reported problems
Philips Ultrasound LLC · Class 2
All models of Transducer X7-2t (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00884838075177), received between Nov 12, 2018 and Nov 7, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Failure to Calibrate” (1 report).
2 FDA recall records name this device's identifier, 2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Recalls naming this device
- Jul 3, 2025Class IIIOpen, Classified
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Z-2412-2025 · Root cause: Device Design · Recall details · FDA record ↗
- May 28, 2025Class IIOpen, Classified
Ultrasound transducer devices were refurbished beyond their useful life.
Z-2066-2025 · Root cause: Process control · Recall details · FDA record ↗
Most reported problems
Device problems
- Failure to Calibrate1
- Mechanical Jam1
- Mechanical Problem1
- Overheating of Device1
- Positioning Problem1
Patient problems
- High Blood Pressure/ Hypertension1
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
- Tachycardia1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 7, 2023Overheating of Device; Failure to Calibrate; Overheating of Device; Failure to Calibrate
A CUSTOMER REPORTED AN INCIDENT WHERE THE X7-2T TRANSDUCER WAS NOT RECOGNIZED AND THEN DISPLAYED A WARNING MESSAGE THAT THE TRANSDUCER WAS OVERHEATING ON THE ULTRASOUND SYSTEM. THE TRANSDUCER WAS REMOVED FROM THE PATIENT. IT WAS ALLEGED THAT THE PATIENT WAS HYPERTENSIVE AND TACHYCARDIC. ADDITIONAL INFORMATION IS BEING GATHERED REGARDING EVENT DETAILS AND ROOT CAUSE OF THE ISSUE WHICH WILL BE INCLUDED IN A FOLLOW UP REPORT.
Patient problems: High Blood Pressure/ Hypertension; Tachycardia
MAUDE report 18085987 ↗MalfunctionFeb 18, 2021Mechanical Problem; Mechanical Jam; Mechanical Problem; Mechanical Jam
A CUSTOMER REPORTED AN X7-2T MODEL TRANSDUCER HAD AN ARTICULATION ISSUE DURING USE. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 11341859 ↗MalfunctionNov 12, 2018Positioning Problem
A CUSTOMER REPORTED AN ARTICULATION ISSUE WITH THEIR X7-2T MODEL TRANSDUCER. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8061143 ↗
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- Site~Rite 8 Ultrasound System 9770600YBard Access Systems, Inc. · System, imaging, pulsed echo, ultrasonic330 reports
- Transducer C9-2 989605391092Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic5 recalls0 reports
- Transducer S5-1 989605412082Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic5 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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