Precision Xceed Pro 70907-03Recalls & reported problems
Abbott Diabetes Care Inc · Precision Xceed Pro Blood Glucose and ?-Ketone Monitoring System · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00357599000189), received between Dec 2, 2020 and Dec 2, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Product Quality 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Product Quality Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 2, 2020Product Quality Problem; Product Quality Problem
A HEALTH CARE PROFESSIONAL REPORTED THAT THE BATTERY OF AN ADC HOSPITAL BLOOD GLUCOSE METER "EXPLODED" WHILE THE METER WAS SITTING ON THE DOCKING STATION. THE HEALTH CARE PROFESSIONAL FURTHER REPORTED THAT THE METER WAS ALSO "VERY HOT TO THE TOUCH." THERE WAS NO REPORT OF A DEATH, SERIOUS INJURY, OR MISTREATMENT ASSOCIATED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10934782 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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