Avalon Toco MP Transducer (REF 867248)Recalls & reported problems
Philips Medizin Systeme Böblingen GmbH · The device is intended to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838093218), received between May 10, 2026 and May 10, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (1 report).
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
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Blister1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 10, 2026Use of Device Problem
IT WAS REPORTED THE PATIENT DEVELOPED BLISTERS UNDER THE TOCO TRANSDUCER. IT WAS NOTED THE CUSTOMER DID NOT USE THE TRANSDUCER BELT BUT USED MICROPORE TAPE TO FIX THE TRANSDUCER TO THE PATIENT'S ABDOMEN. IN ADDITION, IT WAS INDICATED THE TRANSDUCER WAS FIXED IN THIS POSITION FOR 18 HOURS WITH NO DEVICE POSITION CHANGES. GOOD FAITH EFFORTS ARE BEING PERFORMED FOR FURTHER INFORMATION.
Patient problems: Blister
MAUDE report 25133612 ↗
Other Monitor, uterine contraction, external (for use in clinic) devices
- Avalon CL Toco+ MP Transducer Avalon Cableless Toco+ MP TransducerPhilips Medizin Systeme Böblingen GmbH · MONITOR, UTERINE CONTRACTION, EXTERNAL (FOR USE IN CLINIC)13 reports
- Avalon TOCO MP TransducerPhilips Medizin Systeme Böblingen GmbH · MONITOR, UTERINE CONTRACTION, EXTERNAL (FOR USE IN CLINIC)8 reports
- Avalon TOCO+ TransducerPhilips Medizin Systeme Böblingen GmbH · MONITOR, UTERINE CONTRACTION, EXTERNAL (FOR USE IN CLINIC)5 reports
- Avalon Fetal & Maternal Patch Avalon CL Fetal & Maternal PatchPhilips Medical Systems Hsg · Monitor, uterine contraction, external (for use in clinic)3 reports
- Avalon CL Fetal & Maternal PodPhilips Medizin Systeme Böblingen GmbH · Monitor, uterine contraction, external (for use in clinic)1 report
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
- 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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