T/Pump TP700CRecalls & reported problems
Stryker Corporation · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327169263), received between Apr 20, 2018 and Jul 2, 2019 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Device Displays Incorrect Message” (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
- Adverse Event Without Identified Device or Use Problem1
- Device Displays Incorrect Message1
- Temperature Problem1
Patient problems
- Burn(s)1
- No Consequences Or Impact To Patient1
- Partial thickness (Second Degree) Burn1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 2, 2019Temperature Problem; Adverse Event Without Identified Device or Use Problem; Temperature Problem
IT WAS REPORTED THAT THE PATIENT WAS USING THE DEVICE HEATING PAD AND WAS FOUND TO HAVE PARTIAL THICKNESS BURNS TO THE BACK. FURTHER INFORMATION HAS NOT BEEN PROVIDED.
Patient problems: Burn(s); Partial thickness (Second Degree) Burn
MAUDE report 8754129 ↗MalfunctionApr 20, 2018Device Displays Incorrect Message
IT WAS REPORTED THAT THE DEVICE HAD NO OVER TEMPERATURE WARNING. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7448342 ↗
Other Pack, hot or cold, water circulating devices
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- DONJOY 11-1422Djo, LLC · Pack, hot or cold, water circulating1 recall1 report
- DONJOY 11-9099Djo, LLC · Pack, hot or cold, water circulating1 recall0 reports
- Micro-Temp LT 749Gentherm Medical, LLC · Pack, Hot Or Cold, Water Circulating1 recall0 reports
- DONJOY 11-1424Djo, LLC · Pack, hot or cold, water circulating1 recall0 reports
- Electri-Cool ll 767Gentherm Medical, LLC · Pack, Hot Or Cold, Water Circulating1 recall0 reports
- T/Pump TP700Stryker Corporation · Pack, hot or cold, water circulating15 reports
- Mul-T-Pad 8002-062-026Stryker Corporation · Pack, hot or cold, water circulating7 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.