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CVS/Pharmacy KD-1760Recalls & reported problems

Woonsocket Prescription Center, Incorporated · A hand-held, battery-powered, electronic instrument designed for oral, under arm or rectal use to to measure a patient's body temperature. The device has a flexible tip and an LCD display. It is designed to take a temperature reading in approximately 5 seconds. This is a reusable device. · Class 2

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 00050428250440), received between Jul 1, 2020 and Jul 1, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (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

  • Incorrect, Inadequate or Imprecise Result or Readings1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 1, 2020Incorrect, Inadequate or Imprecise Result or Readings

    FALSE READINGS ON DEVICE; WHILE PROVIDING HOME CARE TO ELDERLY PATIENT, A BRAND NEW CVS HEALTH-BRANDED DIGITAL THERMOMETER PROVIDED INCONSISTENT AND QUESTIONABLE TEMPERATURE READINGS. REPLACED THE BATTERY WITH A FRESH ONE, PROBLEM APPEARED TO RESOLVE FOR SEVERAL HOURS AND THEN RETURNED. (B)(6) SEARCH REVEALED MANY IDENTICAL OR SIMILAR PROBLEMS WITH THESE THERMOMETERS, INDICATING A POTENTIAL MANUFACTURING QUALITY PROBLEM. FDA SAFETY REPORT ID# (B)(4).

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10224014 ↗

Other Thermometer, Electronic, Clinical devices

All Thermometer, Electronic, Clinical devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.