Welch Allyn, Inc. 901067 (REF 44900-C)Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn Green Series 900 Procedure Light with Ceiling Mount; 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 00732094004571), received between Jun 19, 2023 and Jun 19, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
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.
MalfunctionJun 19, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE GS900 CEILING MOUNT SUSTAINED PHYSICAL DAMAGE TO THE SWING ARM. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17152345 ↗
Other Light, headband, surgical devices
- Integra® Duo 90620USIntegra Lifesciences (Ireland) Limited · Light, headband, surgical33 reports
- Integra® Duo 90600Integra Lifesciences (Ireland) Limited · Light, headband, surgical10 reports
- Integra® Duo 90622Integra Lifesciences (Ireland) Limited · Light, headband, surgical2 reports
- Integra® 90500Integra Lifesciences Production Corporation · Light, headband, surgical1 report
- Welch Allyn, Inc. 901069Welch Allyn, Inc. · Light, headband, surgical1 report
- Integra® 90520USIntegra Lifesciences Production Corporation · Light, headband, surgical1 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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