NA 399.20Recalls & reported problems
Synthes GmbH · HOHMANN RETRACTOR 8MM SHORT NARROW TIP 220MM · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10886982202550), received between Apr 16, 2024 and Apr 16, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (3 reports).
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
- Contamination /Decontamination Problem3
- Corroded3
- Material Integrity Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 16, 2024Corroded; Contamination /Decontamination Problem; Material Integrity Problem; Corroded; Contamination /Decontamination Problem; Material Integrity Problem
IT WAS FURTHER REPORTED THAT THE CUSTOMER NOTICED SOME POINTS OF CORROSION AT THE LEVEL OF THE ARTICLE AND LOT NUMBER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19119229 ↗MalfunctionApr 16, 2024Corroded; Contamination /Decontamination Problem; Material Integrity Problem; Corroded; Contamination /Decontamination Problem; Material Integrity Problem
IT WAS FURTHER REPORTED THAT THE CUSTOMER NOTICED SOME POINTS OF CORROSION AT THE LEVEL OF THE ARTICLE AND LOT NUMBER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19119228 ↗MalfunctionApr 16, 2024Corroded; Contamination /Decontamination Problem; Material Integrity Problem; Corroded; Contamination /Decontamination Problem; Material Integrity Problem
IT WAS FURTHER REPORTED THAT THE CUSTOMER NOTICED SOME POINTS OF CORROSION AT THE LEVEL OF THE ARTICLE AND LOT NUMBER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19119224 ↗
Other RETRACTOR devices
- Endo Paddle Retract 173046Covidien LP · RETRACTOR56 reports
- Omni-Tract® 4040Integra Lifesciences Corporation · RETRACTOR1 recall3 reports
- CHARNLEY 9620-04-000Depuy International Ltd · RETRACTOR1 recall2 reports
- RadiaLux™ 50-101-1Medtronic Navigation, Inc. · RETRACTOR1 recall2 reports
- Omni-Tract® 11275Integra Lifesciences Corporation · RETRACTOR1 recall2 reports
- NA 2176-10-000Depuy (Ireland) · RETRACTOR51 reports
- Fathom MR2-102050Seaspine Orthopedics Corporation · RETRACTOR1 recall1 report
- Omni-Tract® 10269Integra Lifesciences Corporation · RETRACTOR1 recall0 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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