Snowden-Pencer 88-9760Recalls & reported problems
Steris Corporation · Snowden-Pencer MIS SNOWDEN-PENCER FIBEROPTIC LIGHT CABLE ACMI/ACMI 3.5MM X 7.5FT · Class 2
- 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 10885403155253), received between May 15, 2024 and May 15, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (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
- Overheating of Device1
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.
MalfunctionMay 15, 2024Overheating of Device; Overheating of Device
THE USER FACILITY REPORTED THAT THE FIBEROPTIC LIGHT CABLE TO THEIR LIGHT SOURCE WAS EMITTING A BURNING SMELL WHILE BEING PLUGGED INTO THE INPUT CONNECTOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19325912 ↗
Other LIGHT, SURGICAL, FIBEROPTIC devices
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- Arthrex® AR-3240-5027Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC30 reports
- Integra® 001388LX9Integra Lifesciences (Ireland) Limited · LIGHT, SURGICAL, FIBEROPTIC7 reports
- N/A FC1SPStryker Corporation · Light, Surgical, Fiberoptic5 reports
- UltraLite® AX2100BIFIntegra Lifesciences (Ireland) Limited · LIGHT, SURGICAL, FIBEROPTIC4 reports
- NA 242387Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC3 reports
- Arthrex® AR-3240-5040Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC3 reports
- NA 242388Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.