Temperature ProbesRecalls & reported problems across all models

We found 3 models of Temperature Probes by Philips Medical Systems Hsg in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Jun 11, 2020 and Jun 11, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

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

Temperature Probes 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.

1. Feb 7, 2022Open, Classified

   Update to instructions for use regarding the cleaning and disinfection process for the reusable probes.

   Z-0926-2022 · Root cause: Device Design · names 3 of these models · Recall details · FDA record ↗

Most reported Temperature Probes problems

Temperature Probes models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Temperature Probes Esophageal/Rectal Temperature Probe

  Thermometer, electronic, clinical
  1 recall1 report
• Temperature Probes Esophageal/Rectal Temperature Probe

  Thermometer, electronic, clinical
  1 recall0 reports
• Temperature Probes Skin Surface Temperature Probe

  Thermometer, electronic, clinical
  1 recall0 reports

Recent Temperature Probes adverse event reports

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

• MalfunctionJun 11, 2020Break

  THE CUSTOMER REPORTED THAT THE PLASTIC PIECE IS BROKEN OF THE TEMPERATURE PROBE. THE DEVICE WAS IN USE ON A PATIENT. THERE WAS NO REPORT OF PATIENT OR USER HARM.

  Patient problems: No Patient Involvement

  MAUDE report 10143506 ↗

Other Philips Medical Systems Hsg products

• Patient Information Center iX3 models · 1,836 reports
• SureSigns VS42 models · 103 reports · 9 recalls
• SureSigns VM62 models · 45 reports · 1 recall
• HeartStart3 models · 14 reports · 1 recall
• SureSigns VM82 models · 14 reports · 1 recall
• SureSigns VS2+2 models · 56 reports
• PageWriter5 models · 39 reports
• SureSigns VSi3 models · 25 reports