Ranger™ 24533 (UDI 00707387781590)Recalls & reported problems
3m Company · 3M™ Ranger™ Fluid Warming Unit, Model 245, 120V-ENG-E, Military , 1 each, 24533 · Class 2
Data updated Oct 13, 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 00707387781590), received between Apr 17, 2025 and Apr 17, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Loss of Osseointegration” (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.
Reports received per month
Most reported problems
Device problems
- Loss of Osseointegration1
Patient problems
- Failure of Implant1
- Inflammation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 17, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Inflammation
MAUDE report 21854303 ↗
Other Warmer, blood, non-electromagnetic radiation devices
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- 3M™ Ranger™ 243553m Company · Warmer, blood, non-electromagnetic radiation64 reports
- Ranger™ 243703m Company · Warmer, blood, non-electromagnetic radiation38 reports
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- 3M™ Ranger™ 243703m Company · Warmer, blood, non-electromagnetic radiation9 reports
- buddy™ Disposable Set (1 Piece) 905-00010PBelmont Instrument Corporation · Warmer, Blood, Non-Electromagnetic Radiation8 reports
- Ranger™ 243553m Company · Warmer, blood, non-electromagnetic radiation6 reports
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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