Ranger™ 24200 (UDI 30608223242002)Recalls & reported problems
3m Company · 3M™ Ranger® Fluid Warming Set, Standard Flow, 10 Per Case 24200 · 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 30608223242002), received between Mar 6, 2017 and Mar 6, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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
- Device Operates Differently Than Expected1
Patient problems
- Air Embolism1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 6, 2017Device Operates Differently Than Expected
DURING SURGERY, THE BUBBLE TRAP DID NOT EFFECTIVELY EXPUNGE AIR, THEREBY CAUSING AN AIR EMBOLISM. A 24200 RANGER FLUID WARMINED SET STD FLOW 10/CS - 3MID - (B)(4).
Patient problems: Air Embolism
MAUDE report 6386796 ↗
Other Warmer, blood, non-electromagnetic radiation devices
- Level 1 8002950Icu Medical, Inc. · Warmer, blood, non-electromagnetic radiation10 deaths931 reports
- Ranger™ 243553m Company · Warmer, blood, non-electromagnetic radiation107 reports
- 3M™ Ranger™ 243553m Company · Warmer, blood, non-electromagnetic radiation64 reports
- Ranger™ 243703m Company · Warmer, blood, non-electromagnetic radiation38 reports
- Ranger™ 243653m Company · Warmer, blood, non-electromagnetic radiation16 reports
- 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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