Welch Allyn, Inc. 901067 (REF 44900)Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn Green Series 900 Procedure Light with Mobile Stand; Six White LEDs, 80,000 LUX @ 24 in/61 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
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00732094073362), received between Oct 31, 2021 and Oct 31, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fitting Problem” (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.
Most reported problems
Device problems
- Fitting Problem1
- Flare or Flash1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 31, 2021Fitting Problem; Flare or Flash; Fitting Problem; Flare or Flash
CUSTOMER REPORTED PHYSICAL DAMAGE THAT OCCURRED ON THEIR POWER CORD FOR THEIR DEVICE AND A FIT ISSUE FOR THE LIGHT. THE CUSTOMER STATES THE LUMINER WILL NOT FIT ON THE END OF THE MOBILE STAND AND THE POWER CORD APPEARS TO BE BURNT. THE DEVICE WAS REQUESTED BACK AND A REPLACEMENT UNIT IS BEING SENT TO THE CUSTOMER, HOWEVER THE CUSTOMER HAS NOT RETURNED THE DEVICE BACK. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12725548 ↗
Other Transformer, endoscope devices
- Welch Allyn, Inc. 901027Welch Allyn, Inc. · TRANSFORMER, ENDOSCOPE1 recall0 reports
- Welch Allyn, Inc. 901027Welch Allyn, Inc. · TRANSFORMER, ENDOSCOPE1 recall0 reports
- Y/C cable MB-631Olympus Medical Systems Corp. · Transformer, Endoscope5 reports
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope2 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
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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