Welch Allyn, Inc. 901067 (REF 44410)Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn Green Series 300 General Exam Light with Wall/Table Mount; One White LED, 20,000 LUX @ 12 in/30 cm, 5,500° K; Touchless Controls; 100-240 V, 50-60 Hz AC, IEC Plug Type-B · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00732094073898), received between Sep 14, 2022 and Jul 10, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fire” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fire1
- Material Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 10, 2024Material Split, Cut or Torn; Material Split, Cut or Torn
CUSTOMER REPORTED THAT THE ELECTRICAL CONNECTOR TO THE LIGHT HAD BROKEN OFF AND THE WIRE WAS EXPOSED.THERE WERE NO INJURIES CAUSED BY THE REPORTED EVENT. THIS COMPLAINT WAS CAPTURED UNDER HILLROM REF (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19708695 ↗MalfunctionSep 14, 2022Fire; Fire
THE CUSTOMER REPORTED THAT THE BASE OF THE GS300 CAUGHT FIRE NEAR THE PLUG WHICH THEN CAUSED THE GOOSENECK OF THE LIGHT TO POP OUT OF THE BASE. THERE WERE NO INJURIES CAUSED BY THE REPORTED EVENT. THIS COMPLAINT WAS CAPTURED UNDER HILLROM REF # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15418272 ↗
Other Transformer, endoscope devices
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- Welch Allyn, Inc. 901027Welch Allyn, Inc. · TRANSFORMER, ENDOSCOPE1 recall0 reports
- Y/C cable MB-631Olympus Medical Systems Corp. · Transformer, Endoscope5 reports
- Welch Allyn, Inc. 901027Welch Allyn, Inc. · Transformer, endoscope2 reports
- Welch Allyn, Inc. 901027Welch Allyn, Inc. · Transformer, endoscope2 reports
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope1 report
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope1 report
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope1 report
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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