Snowden-Pencer 88-1090Recalls & reported problems
Steris Corporation · Snowden-Pencer Plastics RETRACTOR TEBBETTS FIBER OPTICS 19CM X 30MM BLADE · Class 1
All models of Snowden-Pencer (62)
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 10885403151682), received between Jul 22, 2022 and Jul 22, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Smoking” (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
- Smoking1
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.
MalfunctionJul 22, 2022Smoking; Smoking
IT WAS REPORTED BY THE CUSTOMER THAT INADEQUATE LIGHT COMING FROM TEBBETTS RETRACTORS. VERBATIM: INADEQUATE LIGHT COMING FROM TEBBETTS RETRACTORS. CUSTOMER HAS (4) EACH OF FOLLOWING: 88-1086, 88-1087, 88-1088 AND 88-1090. ADDITIONAL INFORMATION: INADEQUATE LIGHT COMING FROM TEBBETTS RETRACTORS. CUSTOMER HAS (4) EACH OF FOLLOWING: 88-1086, 88-1087, 88-1088 AND 88-1090. JUST FOR SOME HISTORY. ONE OF THE SURGEONS A WEEK OR 2 AGO HAD ISSUE WITH LACK OF ILLUMINATION WHEN USING THE RETRACTOR SET. I (BIOMED) RESPONDED AND FOUND THAT THEY WERE USING A KARL STORZ LIGHT SOURCE WITH A 4-WAY TURRET ON IT. GENERALLY, THIS TURRET ALLOWS FOR CONNECTION OF 4 DIFFERENT MANUFACTURER¿S LIGHT CABLES HOWEVER, THE SNOWDEN PENCER CABLE DOES NOT POSITIVELY MATCH UP TO ANY OF THEM. THE LIGHT SOURCE ITSELF WAS RUNNING AT 100% INTENSITY AND 43 HRS OF A 500 HR BULB LIFE. THE NURSE WAS ATTEMPTING TO HOLD YOUR3MM CABLE INTO ONE OF THE HOLES ON THE TURRET. JUST MOVING THE CABLE AROUND IN THAT TURRET HAS SOME EFFECT ON THE AMOUNT OF LIGHT GETTING TO THE RETRACTOR. I HAD SUGGESTED THEY TRY TO USE OUR ¿NEW¿ STRYKER LED LIGHT SOURCE AS AT LEAST IT ACCEPTS YOUR CABLE BETTER AND HOLDS IT IN PLACE POSITIVELY. AFTER THE
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15089275 ↗
Other RETRACTOR, FIBEROPTIC devices
- Snowden-Pencer 88-1087Steris Corporation · RETRACTOR, FIBEROPTIC3 reports
- InnerVision® 1465-50Diversatek Healthcare, Inc. · Retractor, Fiberoptic3 reports
- Snowden-Pencer 88-1088Steris Corporation · RETRACTOR, FIBEROPTIC2 reports
- Snowden-Pencer 88-1086Steris Corporation · RETRACTOR, FIBEROPTIC2 reports
- NA 03.612.031Synthes GmbH · RETRACTOR, FIBEROPTIC1 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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